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<!--
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||
UID=52961
|
||
ConceptID=C0042164
|
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-->
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||
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Uveitis</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>52961</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0042164</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Uveitides</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Uveitis (128473001); Intraocular inflammation (128473001)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0000554">HP:0000554</a></td></tr>
|
||
<tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0020283" target="_blank">MONDO:0020283</a></td></tr>
|
||
<tr><td>Orphanet:</td>
|
||
<td><a target="_blank" title="Orphanet: The portal for rare diseases and orphan drugs" href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=98715">ORPHA98715</a></td></tr></tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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<div class="portlet mgSection" id="ID_100">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">Inflammation of one or all portions of the uveal tract. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
|
||
</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li><li><a href="#tabORDO">Orphanet</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0042164[DISCUI]&test_type=Clinical" ref="ncbi_uid=52961">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Uveitis</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/867443" ref="tree=MeSH" title="MedGen record for Phenotypic abnormality">Phenotypic abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/867388" ref="tree=MeSH" title="MedGen record for Abnormality of the immune system">Abnormality of the immune system</a></span><ul><li><span class="TLline"><a href="/medgen/869194" ref="tree=MeSH" title="MedGen record for Abnormality of immune system physiology">Abnormality of immune system physiology</a></span><ul><li><span class="TLline"><a href="/medgen/868411" ref="tree=MeSH" title="MedGen record for Abnormal inflammatory response">Abnormal inflammatory response</a></span><ul><li><span class="TLline"><a href="/medgen/868409" ref="tree=MeSH" title="MedGen record for Increased inflammatory response">Increased inflammatory response</a></span><ul><li><span class="TLline"><a href="/medgen/866622" ref="tree=MeSH" title="MedGen record for Inflammatory abnormality of the eye">Inflammatory abnormality of the eye</a></span><ul><li><span class="matched_ds">Uveitis</span><ul><li><span class="TLline"><a href="/medgen/22595" ref="tree=MeSH" title="MedGen record for Anterior uveitis">Anterior uveitis</a></span><ul><li><span class="TLline"><a href="/medgen/472531" ref="tree=MeSH" title="MedGen record for Acute anterior uveitis">Acute anterior uveitis</a></span></li><li><span class="TLline"><a href="/medgen/2568" ref="tree=MeSH" title="MedGen record for Behcet disease">Behcet disease</a></span></li><li><span class="TLline"><a href="/medgen/573079" ref="tree=MeSH" title="MedGen record for Idiopathic anterior uveitis">Idiopathic anterior uveitis</a></span></li><li><span class="TLline"><a href="/medgen/509716" ref="tree=MeSH" title="MedGen record for Infectious anterior uveitis">Infectious anterior uveitis</a></span></li><li><span class="TLline"><a href="/medgen/43961" ref="tree=MeSH" title="MedGen record for Iridocyclitis">Iridocyclitis</a></span><ul><li><span class="TLline"><a href="/medgen/307139" ref="tree=MeSH" title="MedGen record for Chronic uveitis">Chronic uveitis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/7160" ref="tree=MeSH" title="MedGen record for Iritis">Iritis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/942" ref="tree=MeSH" title="MedGen record for Chorioretinitis">Chorioretinitis</a></span><ul><li><span class="TLline"><a href="/medgen/340098" ref="tree=MeSH" title="MedGen record for Birdshot chorioretinopathy">Birdshot chorioretinopathy</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/22596" ref="tree=MeSH" title="MedGen record for Intermediate uveitis">Intermediate uveitis</a></span><ul><li><span class="TLline"><a href="/medgen/14623" ref="tree=MeSH" title="MedGen record for Pars planitis">Pars planitis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/870351" ref="tree=MeSH" title="MedGen record for Nongranulomatous uveitis">Nongranulomatous uveitis</a></span></li><li><span class="TLline"><a href="/medgen/45303" ref="tree=MeSH" title="MedGen record for Panuveitis">Panuveitis</a></span><ul><li><span class="TLline"><a href="/medgen/1633708" ref="tree=MeSH" title="MedGen record for Idiopathic panuveitis">Idiopathic panuveitis</a></span></li><li><span class="TLline"><a href="/medgen/1669541" ref="tree=MeSH" title="MedGen record for Idiopathic uveal effusion syndrome">Idiopathic uveal effusion syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1684863" ref="tree=MeSH" title="MedGen record for Infectious panuveitis">Infectious panuveitis</a></span></li><li><span class="TLline"><a href="/medgen/22597" ref="tree=MeSH" title="MedGen record for Posterior uveitis">Posterior uveitis</a></span><ul><li><span class="TLline"><a href="/medgen/40282" ref="tree=MeSH" title="MedGen record for Choroiditis">Choroiditis</a></span></li><li><span class="TLline"><a href="/medgen/735629" ref="tree=MeSH" title="MedGen record for White dot syndrome">White dot syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/45203" ref="tree=MeSH" title="MedGen record for Sympathetic ophthalmia">Sympathetic ophthalmia</a></span></li><li><span class="TLline"><a href="/medgen/22599" ref="tree=MeSH" title="MedGen record for Vogt-Koyanagi-Harada disease">Vogt-Koyanagi-Harada disease</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/22598" ref="tree=MeSH" title="MedGen record for Suppurative uveitis">Suppurative uveitis</a></span><ul><li><span class="TLline"><a href="/medgen/10561" ref="tree=MeSH" title="MedGen record for Panophthalmitis">Panophthalmitis</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div><div id="tabORDO">Follow <a target="_blank" href="http://www.orpha.net/consor/cgi-bin/Disease_Classif.php?lng=EN&data_id=156&PatId=13732&search=Disease_Classif_Simple&new=1" class="ital bold">this link</a> to review classifications for <span class="ital">Uveitis</span> in Orphanet.</div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_112">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_7049"><div><strong>Incontinentia pigmenti syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>7049</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information."><span class="highlight" style="background-color:">C0021171</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Incontinentia pigmenti (IP) is a disorder that affects the skin, hair, teeth, nails, eyes, and central nervous system; it occurs primarily in females and on occasion in males. Characteristic skin lesions evolve through four stages: I.. Blistering (birth to age ~4 months). II.. Wart-like rash (for several months). III.. Swirling macular hyperpigmentation (age ~6 months into adulthood). IV.. Linear hypopigmentation. Alopecia, hypodontia, abnormal tooth shape, and dystrophic nails are observed. Neovascularization of the retina, present in some individuals, predisposes to retinal detachment. Neurologic findings including seizures, intellectual disability, and developmental delays are occasionally seen.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/7049">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_66167"><div><strong>Proliferative vitreoretinopathy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>66167</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0242852</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Vitreoretinal membrane shrinkage or contraction secondary to the proliferation of primarily retinal pigment epithelial cells and glial cells, particularly fibrous astrocytes, followed by membrane formation. The formation of fibrillar collagen and cellular proliferation appear to be the basis for the contractile properties of the epiretinal and vitreous membranes.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/66167">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_98370"><div><strong>Chronic infantile neurological, cutaneous and articular syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>98370</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0409818</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Chronic infantile neurologic cutaneous and articular syndrome (CINCA) is an early-onset, severe, chronic inflammatory disease, characterized by cutaneous symptoms, central nervous system involvement, and arthropathy (Feldmann et al., 2002). See also familial cold autoinflammatory syndrome-1 (FCAS1, CAPS1; 120100), an allelic disorder with a less severe phenotype.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/98370">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_167236"><div><strong>Oculodentodigital dysplasia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>167236</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0812437</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Oculodentodigital dysplasia (ODDD) is characterized by a typical facial appearance and variable involvement of the eyes, dentition, and fingers. Characteristic facial features include a narrow, pinched nose with hypoplastic alae nasi, prominent columella and thin anteverted nares together with a narrow nasal bridge, and prominent epicanthic folds giving the impression of hypertelorism. The teeth are usually small and carious. Typical eye findings include microphthalmia and microcornea. The characteristic digital malformation is complete syndactyly of the fourth and fifth fingers (syndactyly type III) but the third finger may be involved and associated camptodactyly is a common finding (summary by Judisch et al., 1979). Neurologic abnormalities are sometimes associated (Gutmann et al., 1991), and lymphedema has been reported in some patients with ODDD (Brice et al., 2013). See review by De Bock et al. (2013). Genetic Heterogeneity of Oculodentodigital Syndrome An autosomal recessive form of ODDD (257850) is also caused by mutation in the GJA1 gene, but the majority of cases are autosomal dominant.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/167236">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_370100"><div><strong>Persistent hyperplastic primary vitreous, autosomal recessive</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>370100</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C1969783</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Persistent hyperplastic primary vitreous (PHPV), also termed 'persistent fetal vasculature,' is a developmental malformation of the eye in which the primary vitreous fails to regress in utero, resulting in the presence of a retrolental fibrovascular membrane with persistence of the posterior portion of the tunica vasculosa lentis and hyaloid artery. This abnormality is usually unilateral and associated with microphthalmia, cataract, glaucoma, and congenital retinal nonattachment (see Haddad et al., 1978; Khaliq et al., 2001; Prasov et al., 2012). PHPV shares phenotypic overlap with Norrie disease (310600). Genetic Heterogeneity of Persistent Hyperplastic Primary Vitreous A dominant form of PHPV has been described (PHPVAD; 611308).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/370100">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_436694"><div><strong>Sarcoidosis, susceptibility to, 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>436694</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C2676468</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Any sarcoidosis in which the cause of the disease is a mutation in the BTNL2 gene.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/436694">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_394568"><div><strong>Sarcoidosis, susceptibility to, 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>394568</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C2697310</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Any sarcoidosis in which the cause of the disease is a mutation in the HLA-DRB1 gene.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/394568">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_811223"><div><strong>Granulomatosis with polyangiitis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>811223</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C3495801</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Granulomatosis with polyangiitis, formerly termed Wegener granulomatosis, is a systemic disease with a complex genetic background. It is characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, vasculitis, and the presence of antineutrophil cytoplasmatic autoantibodies (ANCAs) in patient sera. These ANCAs are antibodies to a defined target antigen, proteinase-3 (PR3, PRTN3; 177020), which is present within primary azurophil granules of neutrophils (PMNs) and lysozymes of monocytes. On cytokine priming of PMNs, PR3 translocates to the cell surface, where PR3-ANCAs can interact with their antigens and activate PMNs. PMNs from patients with active GPA express PR3 on their surface, produce respiratory burst, and release proteolytic enzymes after activation with PR3-ANCAs. The consequence is a self-sustaining inflammatory process (Jagiello et al., 2004).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/811223">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_766426"><div><strong>Combined immunodeficiency due to LRBA deficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>766426</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C3553512</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Common variable immunodeficiency-8 with autoimmunity is an autosomal recessive disorder of immune dysregulation. Affected individuals have early childhood onset of recurrent infections, particularly respiratory infections, and also develop variable autoimmune disorders, including idiopathic thrombocytopenic purpura, autoimmune hemolytic anemia, and inflammatory bowel disease. The presentation and phenotype are highly variable, even within families (summary by Lopez-Herrera et al., 2012 and Alangari et al., 2012). Immunologic findings are also variable and may include decreased B cells, hypogammaglobulinemia, and deficiency of CD4+ T regulatory (Treg) cells (Charbonnier et al., 2015). For a general description and a discussion of genetic heterogeneity of common variable immunodeficiency, see CVID1 (607594).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/766426">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_767454"><div><strong>Lymphoproliferative syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>767454</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C3554540</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Lymphoproliferative syndrome-2, also known as CD27 deficiency, is an autosomal recessive immunodeficiency disorder associated with persistent symptomatic EBV viremia, hypogammaglobulinemia, and impairment in specific antibody function resulting from impaired T cell-dependent B-cell responses and T-cell dysfunction (summary by van Montfrans et al., 2012). The phenotype can vary significantly, from asymptomatic borderline-low hypogammaglobulinemia, to a full-blown symptomatic systemic inflammatory response with life-threatening EBV-related complications, including hemophagocytic lymphohistiocytosis, a lymphoproliferative disorder, and malignant lymphoma requiring stem cell transplantation (summary by Salzer et al., 2013). For a discussion of genetic heterogeneity of lymphoproliferative syndrome, see XLP1 (308240).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/767454">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_934587"><div><strong>Yao syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934587</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C4310620</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Yao syndrome (YAOS) is an autoinflammatory disease characterized by periodic fever, dermatitis, arthritis, and swelling of the distal extremities, as well as gastrointestinal and sicca-like symptoms. The disorder is associated with specific NOD2 variants (and Shen, 2017).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/934587">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1380109"><div><strong>Autoinflammation with arthritis and dyskeratosis</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1380109</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C4479278</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autoinflammation with arthritis and dyskeratosis (AIADK) is characterized by recurrent fever, widespread skin dyskeratosis, arthritis, elevated biologic markers of inflammation, and mild autoimmunity with a high transitional B-cell level (summary by Grandemange et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1380109">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1647324"><div><strong>Familial cold autoinflammatory syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1647324</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C4551895</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Cryopyrin-associated periodic syndromes (CAPS) are a group of conditions that have overlapping signs and symptoms and the same genetic cause. The group includes three conditions known as familial cold autoinflammatory syndrome type 1 (FCAS1), Muckle-Wells syndrome (MWS), and neonatal-onset multisystem inflammatory disorder (NOMID). These conditions were once thought to be distinct disorders but are now considered to be part of the same condition spectrum. FCAS1 is the least severe form of CAPS, MWS is intermediate in severity, and NOMID is the most severe form.\n\nThe signs and symptoms of CAPS affect multiple body systems. Generally, CAPS are characterized by periodic episodes of skin rash, fever, and joint pain. These episodes can be triggered by exposure to cold temperatures, fatigue, other stressors, or they may arise spontaneously. Episodes can last from a few hours to several days. These episodes typically begin in infancy or early childhood and persist throughout life.\n\nWhile the CAPS spectrum shares similar signs and symptoms, the individual conditions tend to have distinct patterns of features. People with FCAS1 are particularly sensitive to the cold, and exposure to cold temperatures can trigger a painful or burning rash. The rash usually affects the torso and limbs but may spread to the rest of the body. In addition to fever and joint pain, other possible symptoms include muscle aches, chills, drowsiness, eye redness, headache, and nausea.\n\nIndividuals with MWS develop the typical periodic episodes of skin rash, fever, and joint pain after cold exposure, although episodes may occur spontaneously or all the time. Additionally, they can develop progressive hearing loss in their teenage years. Other features of MWS include skin lesions or kidney damage from abnormal deposits of a protein called amyloid (amyloidosis).\n\nIn people with NOMID, the signs and symptoms of the condition are usually present from birth and persists throughout life. In addition to skin rash and fever, affected individuals may have joint inflammation, swelling, and joint deformities called contractures that may restrict movement. People with NOMID typically have headaches, seizures, and cognitive impairment resulting from chronic meningitis, which is inflammation of the tissue that covers and protects the brain and spinal cord (meninges). Other features of NOMID include eye problems, short stature, distinctive facial features, and kidney damage caused by amyloidosis.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1647324">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1684759"><div><strong>Blau syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1684759</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C5201146</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Blau syndrome is characterized by the triad of granulomatous arthritis, uveitis, and dermatitis. First described in 1985, it was considered to be distinct from sarcoidosis due to the early age of onset and autosomal dominant inheritance pattern. Published reports of sporadic cases of children with 'early-onset sarcoidosis' (EOS) with granulomatous involvement of different organs, primarily affecting joints, eyes, and skin, were suspected to represent the same disorder because the patients' characteristics were nearly identical. Subsequently, identical NOD2 mutations were identified in patients with Blau syndrome as well as in patients diagnosed with EOS, confirming earlier suspicions that they represented the same disease (summary by Borzutzky et al., 2010). Unlike older children diagnosed with sarcoidosis, these patients have no apparent pulmonary involvement; however, the disease is progressive and may result in severe complications such as blindness and/or joint destruction (Shetty and Gedalia, 1998).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1684759">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1814561"><div><strong>Transketolase deficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1814561</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C5700245</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A rare disorder of pentose phosphate metabolism with characteristics of developmental delay and intellectual disability, delayed or absent speech, short stature and congenital heart defects (such as ventricular septal defect, atrial septal defect and patent foramen ovale). Additional reported features include hypotonia, hyperactivity, stereotypic behaviour, ophthalmologic abnormalities (bilateral cataract, uveitis, strabismus), hearing impairment and variable facial dysmorphism among others. Laboratory analysis shows elevated plasma and urinary polyols (erythritol, arabitol and ribitol) and urinary sugar-phosphates (ribose-5-phosphate and xylulose/ribulose-5-phosphate).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1814561">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1380109" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autoinflammation with arthritis and dyskeratosis</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1684759" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Blau syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_98370" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Chronic infantile neurological, cutaneous and articular syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_766426" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Combined immunodeficiency due to LRBA deficiency</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1647324" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Familial cold autoinflammatory syndrome 1</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (15)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_811223" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Granulomatosis with polyangiitis</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_7049" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Incontinentia pigmenti syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_767454" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Lymphoproliferative syndrome 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_167236" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Oculodentodigital dysplasia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_370100" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Persistent hyperplastic primary vitreous, autosomal recessive</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_66167" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Proliferative vitreoretinopathy</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_394568" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Sarcoidosis, susceptibility to, 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_436694" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Sarcoidosis, susceptibility to, 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1814561" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Transketolase deficiency</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934587" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Yao syndrome</a></div></span></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
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||
<div class="nl"><a target="_blank" href="/pubmed/38499325">EULAR recommendations for the management of psoriatic arthritis with pharmacological therapies: 2023 update.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gossec L,
|
||
Kerschbaumer A,
|
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Ferreira RJO,
|
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Aletaha D,
|
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Baraliakos X,
|
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Bertheussen H,
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Boehncke WH,
|
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Esbensen BA,
|
||
McInnes IB,
|
||
McGonagle D,
|
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Winthrop KL,
|
||
Balanescu A,
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Balint PV,
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||
Burmester GR,
|
||
Cañete JD,
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Claudepierre P,
|
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Eder L,
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Hetland ML,
|
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Iagnocco A,
|
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Kristensen LE,
|
||
Lories R,
|
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Queiro R,
|
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Mauro D,
|
||
Marzo-Ortega H,
|
||
Mease PJ,
|
||
Nash P,
|
||
Wagenaar W,
|
||
Savage L,
|
||
Schett G,
|
||
Shoop-Worrall SJW,
|
||
Tanaka Y,
|
||
Van den Bosch FE,
|
||
van der Helm-van Mil A,
|
||
Zabotti A,
|
||
van der Heijde D,
|
||
Smolen JS</span><br />
|
||
<span class="medgenPMjournal">Ann Rheum Dis</span>
|
||
2024 May 15;83(6):706-719.
|
||
doi: 10.1136/ard-2024-225531.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38499325" target="_blank">38499325</a><a href="/pmc/articles/PMC11103320" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34358489">Extraintestinal Manifestations of Inflammatory Bowel Disease: Current Concepts, Treatment, and Implications for Disease Management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rogler G,
|
||
Singh A,
|
||
Kavanaugh A,
|
||
Rubin DT</span><br />
|
||
<span class="medgenPMjournal">Gastroenterology</span>
|
||
2021 Oct;161(4):1118-1132.
|
||
Epub 2021 Aug 3
|
||
doi: 10.1053/j.gastro.2021.07.042.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34358489" target="_blank">34358489</a><a href="/pmc/articles/PMC8564770" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30282764">Lyme disease: diagnosis and management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ross Russell AL,
|
||
Dryden MS,
|
||
Pinto AA,
|
||
Lovett JK</span><br />
|
||
<span class="medgenPMjournal">Pract Neurol</span>
|
||
2018 Dec;18(6):455-464.
|
||
Epub 2018 Oct 3
|
||
doi: 10.1136/practneurol-2018-001998.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30282764" target="_blank">30282764</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22uveitis%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (1192)</a></div></div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34181974">Pediatric uveitis: A comprehensive review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Maleki A,
|
||
Anesi SD,
|
||
Look-Why S,
|
||
Manhapra A,
|
||
Foster CS</span><br />
|
||
<span class="medgenPMjournal">Surv Ophthalmol</span>
|
||
2022 Mar-Apr;67(2):510-529.
|
||
Epub 2021 Jun 25
|
||
doi: 10.1016/j.survophthal.2021.06.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34181974" target="_blank">34181974</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34431877">Treatment of noninfectious uveitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ferreira LB,
|
||
Farrall AL,
|
||
Furtado JM,
|
||
Smith JR</span><br />
|
||
<span class="medgenPMjournal">Arq Bras Oftalmol</span>
|
||
2021 Nov-Dec;84(6):610-621.
|
||
doi: 10.5935/0004-2749.20220094.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34431877" target="_blank">34431877</a><a href="/pmc/articles/PMC11884374" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27467180">A Focus on the Epidemiology of Uveitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tsirouki T,
|
||
Dastiridou A,
|
||
Symeonidis C,
|
||
Tounakaki O,
|
||
Brazitikou I,
|
||
Kalogeropoulos C,
|
||
Androudi S</span><br />
|
||
<span class="medgenPMjournal">Ocul Immunol Inflamm</span>
|
||
2018;26(1):2-16.
|
||
Epub 2016 Jul 28
|
||
doi: 10.1080/09273948.2016.1196713.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27467180" target="_blank">27467180</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16196117">Standardization of uveitis nomenclature for reporting clinical data. Results of the First International Workshop.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jabs DA,
|
||
Nussenblatt RB,
|
||
Rosenbaum JT;
|
||
Standardization of Uveitis Nomenclature (SUN) Working Group</span><br />
|
||
<span class="medgenPMjournal">Am J Ophthalmol</span>
|
||
2005 Sep;140(3):509-16.
|
||
doi: 10.1016/j.ajo.2005.03.057.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16196117" target="_blank">16196117</a><a href="/pmc/articles/PMC8935739" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12434487">Uveitic glaucoma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kok H,
|
||
Barton K</span><br />
|
||
<span class="medgenPMjournal">Ophthalmol Clin North Am</span>
|
||
2002 Sep;15(3):375-87, viii.
|
||
doi: 10.1016/s0896-1549(02)00028-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12434487" target="_blank">12434487</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Uveitis%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (7643)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38245371">Ocular Sarcoidosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rosenbaum JT,
|
||
Pasadhika S</span><br />
|
||
<span class="medgenPMjournal">Clin Chest Med</span>
|
||
2024 Mar;45(1):59-70.
|
||
Epub 2023 Sep 1
|
||
doi: 10.1016/j.ccm.2023.08.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38245371" target="_blank">38245371</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32823396">Drug-induced uveitis: A review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Agarwal M,
|
||
Dutta Majumder P,
|
||
Babu K,
|
||
Konana VK,
|
||
Goyal M,
|
||
Touhami S,
|
||
Stanescu-Segall D,
|
||
Bodaghi B</span><br />
|
||
<span class="medgenPMjournal">Indian J Ophthalmol</span>
|
||
2020 Sep;68(9):1799-1807.
|
||
doi: 10.4103/ijo.IJO_816_20.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32823396" target="_blank">32823396</a><a href="/pmc/articles/PMC7690475" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27467180">A Focus on the Epidemiology of Uveitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tsirouki T,
|
||
Dastiridou A,
|
||
Symeonidis C,
|
||
Tounakaki O,
|
||
Brazitikou I,
|
||
Kalogeropoulos C,
|
||
Androudi S</span><br />
|
||
<span class="medgenPMjournal">Ocul Immunol Inflamm</span>
|
||
2018;26(1):2-16.
|
||
Epub 2016 Jul 28
|
||
doi: 10.1080/09273948.2016.1196713.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27467180" target="_blank">27467180</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16196117">Standardization of uveitis nomenclature for reporting clinical data. Results of the First International Workshop.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jabs DA,
|
||
Nussenblatt RB,
|
||
Rosenbaum JT;
|
||
Standardization of Uveitis Nomenclature (SUN) Working Group</span><br />
|
||
<span class="medgenPMjournal">Am J Ophthalmol</span>
|
||
2005 Sep;140(3):509-16.
|
||
doi: 10.1016/j.ajo.2005.03.057.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16196117" target="_blank">16196117</a><a href="/pmc/articles/PMC8935739" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12434487">Uveitic glaucoma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kok H,
|
||
Barton K</span><br />
|
||
<span class="medgenPMjournal">Ophthalmol Clin North Am</span>
|
||
2002 Sep;15(3):375-87, viii.
|
||
doi: 10.1016/s0896-1549(02)00028-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12434487" target="_blank">12434487</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Uveitis%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (8674)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36649967">Efficacy and safety of bimekizumab in axial spondyloarthritis: results of two parallel phase 3 randomised controlled trials.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">van der Heijde D,
|
||
Deodhar A,
|
||
Baraliakos X,
|
||
Brown MA,
|
||
Dobashi H,
|
||
Dougados M,
|
||
Elewaut D,
|
||
Ellis AM,
|
||
Fleurinck C,
|
||
Gaffney K,
|
||
Gensler LS,
|
||
Haroon N,
|
||
Magrey M,
|
||
Maksymowych WP,
|
||
Marten A,
|
||
Massow U,
|
||
Oortgiesen M,
|
||
Poddubnyy D,
|
||
Rudwaleit M,
|
||
Shepherd-Smith J,
|
||
Tomita T,
|
||
Van den Bosch F,
|
||
Vaux T,
|
||
Xu H</span><br />
|
||
<span class="medgenPMjournal">Ann Rheum Dis</span>
|
||
2023 Apr;82(4):515-526.
|
||
Epub 2023 Jan 17
|
||
doi: 10.1136/ard-2022-223595.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36649967" target="_blank">36649967</a><a href="/pmc/articles/PMC10086273" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33549728">"Therapeutic uses of natural astaxanthin: An evidence-based review focused on human clinical trials".</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Donoso A,
|
||
González-Durán J,
|
||
Muñoz AA,
|
||
González PA,
|
||
Agurto-Muñoz C</span><br />
|
||
<span class="medgenPMjournal">Pharmacol Res</span>
|
||
2021 Apr;166:105479.
|
||
Epub 2021 Feb 4
|
||
doi: 10.1016/j.phrs.2021.105479.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33549728" target="_blank">33549728</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26501229">Sirolimus for Retinal and Uveitic Diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Agarwal A,
|
||
Rajagopalan N,
|
||
Hassan M,
|
||
Sadiq MA,
|
||
Soliman MK,
|
||
Afridi R,
|
||
Sepah YJ,
|
||
Nguyen QD</span><br />
|
||
<span class="medgenPMjournal">Dev Ophthalmol</span>
|
||
2016;55:276-81.
|
||
Epub 2015 Oct 26
|
||
doi: 10.1159/000438951.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26501229" target="_blank">26501229</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25648267">Secukinumab: first global approval.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sanford M,
|
||
McKeage K</span><br />
|
||
<span class="medgenPMjournal">Drugs</span>
|
||
2015 Feb;75(3):329-38.
|
||
doi: 10.1007/s40265-015-0359-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25648267" target="_blank">25648267</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23143785">Therapeutic roles of curcumin: lessons learned from clinical trials.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gupta SC,
|
||
Patchva S,
|
||
Aggarwal BB</span><br />
|
||
<span class="medgenPMjournal">AAPS J</span>
|
||
2013 Jan;15(1):195-218.
|
||
Epub 2012 Nov 10
|
||
doi: 10.1208/s12248-012-9432-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23143785" target="_blank">23143785</a><a href="/pmc/articles/PMC3535097" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Uveitis%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (7092)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34147542">Ocular syphilis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Furtado JM,
|
||
Simões M,
|
||
Vasconcelos-Santos D,
|
||
Oliver GF,
|
||
Tyagi M,
|
||
Nascimento H,
|
||
Gordon DL,
|
||
Smith JR</span><br />
|
||
<span class="medgenPMjournal">Surv Ophthalmol</span>
|
||
2022 Mar-Apr;67(2):440-462.
|
||
Epub 2021 Jun 18
|
||
doi: 10.1016/j.survophthal.2021.06.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34147542" target="_blank">34147542</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27467180">A Focus on the Epidemiology of Uveitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tsirouki T,
|
||
Dastiridou A,
|
||
Symeonidis C,
|
||
Tounakaki O,
|
||
Brazitikou I,
|
||
Kalogeropoulos C,
|
||
Androudi S</span><br />
|
||
<span class="medgenPMjournal">Ocul Immunol Inflamm</span>
|
||
2018;26(1):2-16.
|
||
Epub 2016 Jul 28
|
||
doi: 10.1080/09273948.2016.1196713.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27467180" target="_blank">27467180</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23217584">Glaucoma and uveitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Siddique SS,
|
||
Suelves AM,
|
||
Baheti U,
|
||
Foster CS</span><br />
|
||
<span class="medgenPMjournal">Surv Ophthalmol</span>
|
||
2013 Jan-Feb;58(1):1-10.
|
||
doi: 10.1016/j.survophthal.2012.04.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23217584" target="_blank">23217584</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20375860">Tuberculous uveitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Abu El-Asrar AM,
|
||
Abouammoh M,
|
||
Al-Mezaine HS</span><br />
|
||
<span class="medgenPMjournal">Int Ophthalmol Clin</span>
|
||
2010 Spring;50(2):19-39.
|
||
doi: 10.1097/IIO.0b013e3181d2ccb9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20375860" target="_blank">20375860</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12848952">The epidemiology of autoimmune diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cooper GS,
|
||
Stroehla BC</span><br />
|
||
<span class="medgenPMjournal">Autoimmun Rev</span>
|
||
2003 May;2(3):119-25.
|
||
doi: 10.1016/s1568-9972(03)00006-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12848952" target="_blank">12848952</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Uveitis%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (4400)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37463464">TECLISTAMAB-ASSOCIATED SCLEROUVEITIS WITH HYPOPYON.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Liu T,
|
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Schwartz T,
|
||
Chebolu AP,
|
||
Tsui JC,
|
||
Bhatt N,
|
||
Scoles D</span><br />
|
||
<span class="medgenPMjournal">Retin Cases Brief Rep</span>
|
||
2024 Sep 1;18(5):580-584.
|
||
doi: 10.1097/ICB.0000000000001449.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37463464" target="_blank">37463464</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34358489">Extraintestinal Manifestations of Inflammatory Bowel Disease: Current Concepts, Treatment, and Implications for Disease Management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rogler G,
|
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Singh A,
|
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Kavanaugh A,
|
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Rubin DT</span><br />
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<span class="medgenPMjournal">Gastroenterology</span>
|
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2021 Oct;161(4):1118-1132.
|
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Epub 2021 Aug 3
|
||
doi: 10.1053/j.gastro.2021.07.042.
|
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<span class="bold">PMID: </span><a href="/pubmed/34358489" target="_blank">34358489</a><a href="/pmc/articles/PMC8564770" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31021540">2019 American College of Rheumatology/Arthritis Foundation Guideline for the Screening, Monitoring, and Treatment of Juvenile Idiopathic Arthritis-Associated Uveitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Angeles-Han ST,
|
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Ringold S,
|
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Beukelman T,
|
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Lovell D,
|
||
Cuello CA,
|
||
Becker ML,
|
||
Colbert RA,
|
||
Feldman BM,
|
||
Holland GN,
|
||
Ferguson PJ,
|
||
Gewanter H,
|
||
Guzman J,
|
||
Horonjeff J,
|
||
Nigrovic PA,
|
||
Ombrello MJ,
|
||
Passo MH,
|
||
Stoll ML,
|
||
Rabinovich CE,
|
||
Sen HN,
|
||
Schneider R,
|
||
Halyabar O,
|
||
Hays K,
|
||
Shah AA,
|
||
Sullivan N,
|
||
Szymanski AM,
|
||
Turgunbaev M,
|
||
Turner A,
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Reston J</span><br />
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<span class="medgenPMjournal">Arthritis Care Res (Hoboken)</span>
|
||
2019 Jun;71(6):703-716.
|
||
Epub 2019 Apr 25
|
||
doi: 10.1002/acr.23871.
|
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<span class="bold">PMID: </span><a href="/pubmed/31021540" target="_blank">31021540</a><a href="/pmc/articles/PMC6777949" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25323655">Drug-induced uveitis.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Cordero-Coma M,
|
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Salazar-Méndez R,
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Garzo-García I,
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Yilmaz T</span><br />
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<span class="medgenPMjournal">Expert Opin Drug Saf</span>
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2015 Jan;14(1):111-26.
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Epub 2014 Oct 17
|
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doi: 10.1517/14740338.2015.972363.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25323655" target="_blank">25323655</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24100371">Drug-induced uveitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Moorthy RS,
|
||
London NJ,
|
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Garg SJ,
|
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Cunningham ET Jr</span><br />
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<span class="medgenPMjournal">Curr Opin Ophthalmol</span>
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2013 Nov;24(6):589-97.
|
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doi: 10.1097/01.icu.0000434534.32063.5c.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24100371" target="_blank">24100371</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Uveitis%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (3730)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/38499325">EULAR recommendations for the management of psoriatic arthritis with pharmacological therapies: 2023 update.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gossec L,
|
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Kerschbaumer A,
|
||
Ferreira RJO,
|
||
Aletaha D,
|
||
Baraliakos X,
|
||
Bertheussen H,
|
||
Boehncke WH,
|
||
Esbensen BA,
|
||
McInnes IB,
|
||
McGonagle D,
|
||
Winthrop KL,
|
||
Balanescu A,
|
||
Balint PV,
|
||
Burmester GR,
|
||
Cañete JD,
|
||
Claudepierre P,
|
||
Eder L,
|
||
Hetland ML,
|
||
Iagnocco A,
|
||
Kristensen LE,
|
||
Lories R,
|
||
Queiro R,
|
||
Mauro D,
|
||
Marzo-Ortega H,
|
||
Mease PJ,
|
||
Nash P,
|
||
Wagenaar W,
|
||
Savage L,
|
||
Schett G,
|
||
Shoop-Worrall SJW,
|
||
Tanaka Y,
|
||
Van den Bosch FE,
|
||
van der Helm-van Mil A,
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||
Zabotti A,
|
||
van der Heijde D,
|
||
Smolen JS</span><br />
|
||
<span class="medgenPMjournal">Ann Rheum Dis</span>
|
||
2024 May 15;83(6):706-719.
|
||
doi: 10.1136/ard-2024-225531.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38499325" target="_blank">38499325</a><a href="/pmc/articles/PMC11103320" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35457041">Vitamin D and Ocular Diseases: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chan HN,
|
||
Zhang XJ,
|
||
Ling XT,
|
||
Bui CH,
|
||
Wang YM,
|
||
Ip P,
|
||
Chu WK,
|
||
Chen LJ,
|
||
Tham CC,
|
||
Yam JC,
|
||
Pang CP</span><br />
|
||
<span class="medgenPMjournal">Int J Mol Sci</span>
|
||
2022 Apr 11;23(8)
|
||
doi: 10.3390/ijms23084226.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35457041" target="_blank">35457041</a><a href="/pmc/articles/PMC9032397" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35233993">2021 American College of Rheumatology Guideline for the Treatment of Juvenile Idiopathic Arthritis: Therapeutic Approaches for Oligoarthritis, Temporomandibular Joint Arthritis, and Systemic Juvenile Idiopathic Arthritis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Onel KB,
|
||
Horton DB,
|
||
Lovell DJ,
|
||
Shenoi S,
|
||
Cuello CA,
|
||
Angeles-Han ST,
|
||
Becker ML,
|
||
Cron RQ,
|
||
Feldman BM,
|
||
Ferguson PJ,
|
||
Gewanter H,
|
||
Guzman J,
|
||
Kimura Y,
|
||
Lee T,
|
||
Murphy K,
|
||
Nigrovic PA,
|
||
Ombrello MJ,
|
||
Rabinovich CE,
|
||
Tesher M,
|
||
Twilt M,
|
||
Klein-Gitelman M,
|
||
Barbar-Smiley F,
|
||
Cooper AM,
|
||
Edelheit B,
|
||
Gillispie-Taylor M,
|
||
Hays K,
|
||
Mannion ML,
|
||
Peterson R,
|
||
Flanagan E,
|
||
Saad N,
|
||
Sullivan N,
|
||
Szymanski AM,
|
||
Trachtman R,
|
||
Turgunbaev M,
|
||
Veiga K,
|
||
Turner AS,
|
||
Reston JT</span><br />
|
||
<span class="medgenPMjournal">Arthritis Rheumatol</span>
|
||
2022 Apr;74(4):553-569.
|
||
Epub 2022 Mar 1
|
||
doi: 10.1002/art.42037.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35233993" target="_blank">35233993</a><a href="/pmc/articles/PMC10161784" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35233986">2021 American College of Rheumatology Guideline for the Treatment of Juvenile Idiopathic Arthritis: Therapeutic Approaches for Oligoarthritis, Temporomandibular Joint Arthritis, and Systemic Juvenile Idiopathic Arthritis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Onel KB,
|
||
Horton DB,
|
||
Lovell DJ,
|
||
Shenoi S,
|
||
Cuello CA,
|
||
Angeles-Han ST,
|
||
Becker ML,
|
||
Cron RQ,
|
||
Feldman BM,
|
||
Ferguson PJ,
|
||
Gewanter H,
|
||
Guzman J,
|
||
Kimura Y,
|
||
Lee T,
|
||
Murphy K,
|
||
Nigrovic PA,
|
||
Ombrello MJ,
|
||
Rabinovich CE,
|
||
Tesher M,
|
||
Twilt M,
|
||
Klein-Gitelman M,
|
||
Barbar-Smiley F,
|
||
Cooper AM,
|
||
Edelheit B,
|
||
Gillispie-Taylor M,
|
||
Hays K,
|
||
Mannion ML,
|
||
Peterson R,
|
||
Flanagan E,
|
||
Saad N,
|
||
Sullivan N,
|
||
Szymanski AM,
|
||
Trachtman R,
|
||
Turgunbaev M,
|
||
Veiga K,
|
||
Turner AS,
|
||
Reston JT</span><br />
|
||
<span class="medgenPMjournal">Arthritis Care Res (Hoboken)</span>
|
||
2022 Apr;74(4):521-537.
|
||
Epub 2022 Mar 1
|
||
doi: 10.1002/acr.24853.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35233986" target="_blank">35233986</a><a href="/pmc/articles/PMC10124899" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31021540">2019 American College of Rheumatology/Arthritis Foundation Guideline for the Screening, Monitoring, and Treatment of Juvenile Idiopathic Arthritis-Associated Uveitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Angeles-Han ST,
|
||
Ringold S,
|
||
Beukelman T,
|
||
Lovell D,
|
||
Cuello CA,
|
||
Becker ML,
|
||
Colbert RA,
|
||
Feldman BM,
|
||
Holland GN,
|
||
Ferguson PJ,
|
||
Gewanter H,
|
||
Guzman J,
|
||
Horonjeff J,
|
||
Nigrovic PA,
|
||
Ombrello MJ,
|
||
Passo MH,
|
||
Stoll ML,
|
||
Rabinovich CE,
|
||
Sen HN,
|
||
Schneider R,
|
||
Halyabar O,
|
||
Hays K,
|
||
Shah AA,
|
||
Sullivan N,
|
||
Szymanski AM,
|
||
Turgunbaev M,
|
||
Turner A,
|
||
Reston J</span><br />
|
||
<span class="medgenPMjournal">Arthritis Care Res (Hoboken)</span>
|
||
2019 Jun;71(6):703-716.
|
||
Epub 2019 Apr 25
|
||
doi: 10.1002/acr.23871.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31021540" target="_blank">31021540</a><a href="/pmc/articles/PMC6777949" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Uveitis%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (218)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
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|
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|
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|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C0042164%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (5)</a></li>
|
||
<li><a href="/gtr/tests?term=C0042164%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (5)</a></li>
|
||
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C0042164%5bDISCUI%5d" target="_blank">See all (5)</a></total></li>
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<div class="portlet_content ln"><ul><li><a href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=98715" target="_blank">Orphanet</a></li><li><a href="https://clinicaltrials.gov/search?cond=Uveitis" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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|
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|
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22uveitis%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Uveitis%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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<div class="portlet_content ln"><ul><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Uveitis" target="_blank">MedlinePlus</a></li><li><a href="https://rarediseases.info.nih.gov/diseases/19549/disease" target="_blank">NCATS Office of Rare Diseases Research (GARD)</a></li></ul></div>
|
||
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|
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