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<!--
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UID=75508
|
||
ConceptID=C0262985
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Psoriasiform dermatitis</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75508</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.">C0262985</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>Psoriasiform eczema</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Psoriasiform eczema (238564003); Psoriasiform dermatitis (52230004)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td><a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#target-gene-loc">Gene (location):<img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a><div class="display-none" id="target-gene-loc">
|
||
Gene(s) directly associated with<br />
|
||
this condition or phenotype.</div></td>
|
||
<td><a target="_blank" title="MSMO1 - ID: 6307 - NCBI Gene" href="/gene/6307" class="medgenPMinfo">MSMO1</a> (4q32.3)</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:0003765">HP:0003765</a></td></tr>
|
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</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_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>
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||
<div class="portlet_content ln">A skin abnormality characterized by redness and irritation, with thick, red skin that displays flaky, silver-white patches (scales). [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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</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>
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<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></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="TLline">Psoriasiform dermatitis</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/21047" ref="tree=MeSH" title="MedGen record for Pathological Conditions, Signs and Symptoms">Pathological Conditions, Signs and Symptoms</a></span><ul><li><span class="TLline"><a href="/medgen/18325" ref="tree=MeSH" title="MedGen record for Pathological process">Pathological process</a></span><ul><li><span class="TLline"><a href="/medgen/4347" ref="tree=MeSH" title="MedGen record for Disease">Disease</a></span><ul><li><span class="TLline"><a href="/medgen/232130" ref="tree=MeSH" title="MedGen record for Disorder by Site">Disorder by Site</a></span><ul><li><span class="TLline"><a href="/medgen/20777" ref="tree=MeSH" title="MedGen record for Skin disorder">Skin disorder</a></span><ul><li><span class="TLline"><a href="/medgen/4233" ref="tree=MeSH" title="MedGen record for Dermatitis">Dermatitis</a></span><ul><li><span class="matched_ds">Psoriasiform dermatitis</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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||
</div>
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||
|
||
<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_7771"><div><strong>Mycosis fungoides</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>7771</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.">C0026948</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Neoplastic Process</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Mycosis fungoides is a malignant T-cell lymphoma of the skin, first reported (and named) by Alibert (1835). Sezary syndrome is a leukemic variant of mycosis fungoides defined by erythroderma with greater than 80% of the skin showing redness, adenopathy and greater than 1,000 circulating Sezary cells/microliter with a CD4+CD26- or CD4+CD7- phenotype. Sezary cells have a type 2 helper T cell cytokine profile. Sezary syndrome has a median overall survival time of only 2.4 years in patients with Sezary cells at a density of greater than 10,000 cells/microliter or 5.4 years in patients with 1,000-10,000 Sezary cells/microliter. Mycosis fungoides and Sezary syndrome are the most common cutaneous T-cell lymphomas. Sezary syndrome can arise de novo or can appear following years of chronic mycosis fungoides. Both are thought to arise from clonal expansion of CD4+ helper T cells responding to chronic antigen stimulation (summary by Wang et al., 2015).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/7771">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_581114"><div><strong>Acrodermatitis continua suppurativa of Hallopeau</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>581114</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.">C0392439</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A rare, genetic, chronic, recurrent, slowly progressive, epidermal disease characterized by small, sterile, pustular eruptions, involving the nails and surrounding skin of the fingers and/or toes, which coalesce and burst, leaving erythematous, atrophic skin where new pustules develop. Onychodystrophy is frequently associated and anonychia and osteolysis are reported in severe cases. Local expansion (to involve the hands, forearms and/or feet) and involvement of mucosal surfaces (e.g. conjunctiva, tongue, urethra) may be observed.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/581114">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_339855"><div><strong>DNA ligase IV deficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>339855</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.">C1847827</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">LIG4 syndrome is an autosomal recessive severe combined immunodeficiency with features of radiosensitivity, chromosomal instability, pancytopenia, and developmental and growth delay. Leukemia and dysmorphic facial features have been reported in some patients (summary by van der Burg et al., 2006).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/339855">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_377894"><div><strong>Immunodeficiency due to CD25 deficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>377894</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.">C1853392</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Immunodeficiency-41 is an autosomal recessive complex disorder of immune dysregulation. Affected individuals present in infancy with recurrent viral, fungal, and bacterial infections, lymphadenopathy, and variable autoimmune features, such as autoimmune enteropathy and eczematous skin lesions. Immunologic studies show a defect in T-cell regulation (summary by Goudy et al., 2013).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/377894">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_400145"><div><strong>Spondyloarthropathy, susceptibility to, 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>400145</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.">C1862852</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Spondyloarthropathy (SpA), one of the commonest chronic rheumatic diseases, includes a spectrum of related disorders comprising the prototype ankylosing spondylitis (AS), a subset of psoriatic arthritis (PsA), reactive arthritis (ReA), arthritis associated with inflammatory bowel disease, and undifferentiated spondyloarthropathy (Miceli-Richard et al., 2004). These phenotypes are difficult to differentiate because they may occur simultaneously or sequentially in the same patient. Studies have suggested that a predominant shared component, including HLA-B27, predisposes to all phenotypic subsets, and that these subsets should be considered as various phenotypic expressions of the same disease (Said-Nahal et al., 2000, Said-Nahal et al., 2001). Braun and Sieper (2007) provided a detailed review of ankylosing spondylitis, including clinical features, pathogenesis, and management. Genetic Heterogeneity of Susceptibility to Spondyloarthropathy Additional susceptibility loci for spondyloarthropathy have been identified on chromosome 9q31-q34 (SPDA2; 183840) and chromosome 2q36 (SPDA3; 613238).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/400145">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_351141"><div><strong>Psoriasis 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>351141</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.">C1864497</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Any psoriasis in which the cause of the disease is a mutation in the CARD14 gene.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/351141">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_357279"><div><strong>Psoriasis 1, susceptibility to</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>357279</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.">C1867449</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Psoriasis (psoriasis vulgaris; PV) is a chronic inflammatory dermatosis that affects approximately 2% of the population. It is characterized by red, scaly skin patches that are usually found on the scalp, elbows, and knees, and may be associated with severe arthritis. The lesions are caused by abnormal keratinocyte proliferation and infiltration of inflammatory cells into the dermis and epidermis. The usual age of onset of psoriasis is between 15 and 30 years, although it can present at any age (summary by Matthews et al., 1996). Generalized pustular psoriasis (GPP) is a life-threatening disease characterized by sudden, repeated episodes of high-grade fever, generalized rash, and disseminated pustules, with hyperleukocytosis and elevated serum levels of C-reactive protein (123260) (summary by Marrakchi et al., 2011). GPP often presents in patients with existing or prior psoriasis vulgaris; however, GPP can develop without a history of PV (Sugiura et al., 2013). Palmoplantar pustulosis and acrodermatitis continua of Hallopeau represent acral forms of pustular psoriasis that have historically been grouped with GPP (summary by Setta-Kaffetzi et al., 2013). Nestle et al. (2009) provided a detailed review of the pathogenesis and genetics of psoriasis. Genetic Heterogeneity of Psoriasis and Psoriasis Susceptibility PSORS2 (602723) is caused by mutation in the CARD14 gene (607211) on chromosome 17q25, and PSORS14 (614204) is caused by mutation in the IL36RN gene (605507) on chromosome 2q14. Psoriasis susceptibility loci include PSORS1 on 6p21.3; PSORS3 (601454) on 4q; PSORS4 on 1q21; PSORS5 (604316) on 3q21; PSORS6 (605364) on 19p; PSORS7 (605606) on 1p; PSORS8 (610707) on 16q; PSORS9 (607857) on 4q31; PSORS10 (612410) on 18p11; PSORS11 (612599) on 5q31-q33; PSORS12 (612950) on 20q13; PSORS13 (614070), conferred by variation in the TRAF3IP2 gene (607043) on 6q21; and PSORS15 (616106), conferred by variation in the AP1S3 gene (615781) on 2q36. An additional putative psoriasis candidate locus has been reported on 20p (Nair et al., 1997).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/357279">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_477139"><div><strong>Multiple congenital anomalies-hypotonia-seizures syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>477139</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.">C3275508</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Multiple congenital anomalies-hypotonia-seizures syndrome-2 (MCAHS2) is an X-linked recessive neurodevelopmental disorder characterized by dysmorphic features, neonatal hypotonia, early-onset myoclonic seizures, and variable congenital anomalies involving the central nervous, cardiac, and urinary systems. Some affected individuals die in infancy (summary by Johnston et al., 2012). The phenotype shows clinical variability with regard to severity and extraneurologic features. However, most patients present in infancy with early-onset epileptic encephalopathy associated with developmental arrest and subsequent severe neurologic disability; these features are consistent with a form of developmental and epileptic encephalopathy (DEE) (summary by Belet et al., 2014, Kato et al., 2014). The disorder is caused by a defect in glycosylphosphatidylinositol (GPI) biosynthesis. For a discussion of genetic heterogeneity of MCAHS, see MCAHS1 (614080). For a discussion of nomenclature and genetic heterogeneity of DEE, see 308350. For a discussion of genetic heterogeneity of GPI biosynthesis defects, see GPIBD1 (610293).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/477139">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_501947"><div><strong>X-linked intellectual disability-seizures-psoriasis syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>501947</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.">C3501539</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A rare, X-linked syndromic intellectual disability disorder characterized by severe intellectual disability, psychomotor developmental delay, generalized seizures, and psoriasis. Mild craniofacial dysmorphism, such as hypertelorism, broad nasal bridge, anteverted nares, macrostomia, highly arched palate and large ears, is also associated. There have been no further descriptions in the literature since 1988.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/501947">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_816049"><div><strong>Severe dermatitis-multiple allergies-metabolic wasting syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>816049</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.">C3809719</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A rare genetic epidermal disorder with characteristics of congenital erythroderma with severe psoriasiform dermatitis, ichthyosis, severe palmoplantar keratoderma, yellow keratosis on the hands and feet, elevated immunoglobulin E, multiple food allergies, and metabolic wasting. Other variable features may include hypotrichosis, nail dystrophy, recurrent infections, mild global developmental delay, eosinophilia, nystagmus, growth impairment and cardiac defects.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/816049">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_816321"><div><strong>Immunodeficiency, common variable, 10</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>816321</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.">C3809991</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Common variable immunodeficiency-10 (CVID10) is an autosomal dominant primary immunodeficiency characterized by childhood-onset of recurrent infections, hypogammaglobulinemia, and decreased numbers of memory and marginal zone B cells. Some patients may develop autoimmune features and have circulating autoantibodies. An unusual feature is central adrenal insufficiency (summary by Chen et al., 2013). 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/816321">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_863651"><div><strong>Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>863651</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.">C4015214</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Immune dysregulation with autoimmunity, immunodeficiency, and lymphoproliferation (IDAIL) is an autosomal dominant complex immune disorder with highly variable presentation and clinical manifestations. Prominent features include recurrent infections often associated with hypogammaglobulinemia, autoimmune features such as autoimmune cytopenias, and abnormal lymphocytic infiltration of nonlymphoid organs, including the lungs, brain, and gastrointestinal tract, resulting in enteropathy. Laboratory studies often show lymphopenia and abnormal T and B cell subsets. The variable features are a result of impaired function of Treg cells, which play a role in immune homeostasis (summary by Kuehn et al., 2014; Schwab et al., 2018, and Lopez-Nevado et al., 2021). The disorder shows overlapping features with autoimmune lymphoproliferative syndrome (ALPS); for a general description and a discussion of genetic heterogeneity of ALPS, see 601859.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/863651">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_863672"><div><strong>Psoriasis 15, pustular, susceptibility to</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>863672</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.">C4015235</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">While many affected individuals have features only of GPP (called GPP alone), some develop features of another skin condition called psoriasis vulgaris (PV), either before or after GPP appears. PV, the most common form of psoriasis, is characterized by red, scaly patches of skin (plaques) on parts of the body.\n\nGeneralized pustular psoriasis (GPP) is a severe form of a skin disorder called psoriasis. GPP and other forms of psoriasis are caused by abnormal inflammation. Inflammation is a normal immune system response to injury and foreign invaders (such as bacteria). However, when inflammation is abnormal and uncontrolled, it can damage the body's tissues and organs. Individuals with GPP have repeated episodes in which large areas of skin become red and inflamed and develop small pus-filled blisters (pustules). The skin problems can be accompanied by fever, extreme tiredness (fatigue), muscle weakness, an increased number of white blood cells, and other signs of inflammation throughout the body (systemic inflammation). The inflammation problems subside and reappear often. Episodes can be triggered by infection, exposure to or withdrawal from certain medications, menstruation, or pregnancy, although the trigger is often unknown. GPP can be life-threatening if not treated.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/863672">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_934623"><div><strong>Immunodeficiency 49</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934623</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.">C4310656</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Any primary immunodeficiency disease in which the cause of the disease is a mutation in the BCL11B gene.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/934623">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1386863"><div><strong>Bleeding disorder, platelet-type, 21</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1386863</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.">C4479515</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">BDPLT21 is a hematologic disorder characterized by increased risk of bleeding resulting from a functional platelet defect. Platelets have decreased or even absent dense bodies and abnormally enlarged and fused alpha-granules, and they show defective secretion and aggregation responses to agonists. Platelets are usually enlarged, and some patients may have mild to moderate thrombocytopenia (summary by Saultier et al., 2017).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1386863">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1614928"><div><strong>Immunodeficiency, common variable, 14</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1614928</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.">C4540380</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1614928">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1798933"><div><strong>Microcephaly-congenital cataract-psoriasiform dermatitis syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1798933</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.">C5567510</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Microcephaly, congenital cataract, and psoriasiform dermatitis (MCCPD) represents an inborn error of cholesterol metabolism that is characterized by accumulation of a large amount of methylsterols, particularly dimethylsterols, in affected patients. The associated features of immune dysregulation, skin disease, and growth delay can be at least partially corrected with cholesterol and statin supplements (He et al., 2014).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1798933">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1806192"><div><strong>Gastrointestinal defects and immunodeficiency syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1806192</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.">C5680044</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Gastrointestinal defects and immunodeficiency syndrome-1 (GIDID1) is characterized by multiple intestinal atresia, in which atresia occurs at various levels throughout the small and large intestines. Surgical outcomes are poor, and the condition is usually fatal within the first month of life. Some patients exhibit inflammatory bowel disease (IBD), with or without intestinal atresia, and in some cases, the intestinal features are associated with either mild or severe combined immunodeficiency (Samuels et al., 2013; Avitzur et al., 2014; Lemoine et al., 2014). Genetic Heterogeneity of GIDID See also GIDID2 (619708), caused by mutation in the PI4KA gene (600286) on chromosome 22q11.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1806192">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_581114" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Acrodermatitis continua suppurativa of Hallopeau</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_863651" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1386863" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Bleeding disorder, platelet-type, 21</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_339855" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">DNA ligase IV deficiency</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1806192" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Gastrointestinal defects and immunodeficiency syndrome 1</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (18)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934623" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Immunodeficiency 49</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_377894" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Immunodeficiency due to CD25 deficiency</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_816321" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Immunodeficiency, common variable, 10</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1614928" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Immunodeficiency, common variable, 14</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1798933" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Microcephaly-congenital cataract-psoriasiform dermatitis syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_477139" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Multiple congenital anomalies-hypotonia-seizures syndrome 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_7771" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mycosis fungoides</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_357279" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Psoriasis 1, susceptibility to</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_863672" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Psoriasis 15, pustular, susceptibility to</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_351141" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Psoriasis 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_816049" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Severe dermatitis-multiple allergies-metabolic wasting syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_400145" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spondyloarthropathy, susceptibility to, 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_501947" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">X-linked intellectual disability-seizures-psoriasis syndrome</a></div></span></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
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||
<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>
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||
<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/38279614">Clinicopathological definition, management and prognostic value of mogamulizumab-associated rash and other cutaneous events: A systematic review.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Avallone G,
|
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Roccuzzo G,
|
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Pileri A,
|
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Agostinelli C,
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Maronese CA,
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Aquino C,
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Tavoletti G,
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Onida F,
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Fava P,
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Ribero S,
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Marzano AV,
|
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Berti E,
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Quaglino P,
|
||
Alberti-Violetti S</span><br />
|
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<span class="medgenPMjournal">J Eur Acad Dermatol Venereol</span>
|
||
2024 Sep;38(9):1738-1748.
|
||
Epub 2024 Jan 26
|
||
doi: 10.1111/jdv.19801.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38279614" target="_blank">38279614</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35760771">Anti-tumour necrosis factor-induced skin rashes in inflammatory bowel disease: a systematic review and evidence-based management algorithm.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Au M,
|
||
Heddle G,
|
||
Young E,
|
||
Ryan E,
|
||
Graf S,
|
||
Tee D,
|
||
Philpott H</span><br />
|
||
<span class="medgenPMjournal">Intern Med J</span>
|
||
2023 Oct;53(10):1854-1865.
|
||
Epub 2022 Sep 30
|
||
doi: 10.1111/imj.15859.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35760771" target="_blank">35760771</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34647354">Psoriasiform dermatitis during dupilumab treatment for moderate-to-severe atopic dermatitis in children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Parker JJ,
|
||
Sugarman JL,
|
||
Silverberg NB,
|
||
Gonzalez ME,
|
||
Ramien ML,
|
||
Teng JMC,
|
||
Paller AS</span><br />
|
||
<span class="medgenPMjournal">Pediatr Dermatol</span>
|
||
2021 Nov;38(6):1500-1505.
|
||
Epub 2021 Oct 14
|
||
doi: 10.1111/pde.14820.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34647354" target="_blank">34647354</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22psoriasiform%20dermatitis%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 (6)</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/39396818">Five-year real-world drug survival of dupilumab in severe atopic dermatitis and associate predictors.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Barei F,
|
||
Calzari P,
|
||
Valtellini L,
|
||
Chiei Gallo A,
|
||
Perego G,
|
||
Tavecchio S,
|
||
Zussino M,
|
||
Marzano AV,
|
||
Ferrucci S</span><br />
|
||
<span class="medgenPMjournal">J Dermatolog Treat</span>
|
||
2024 Dec;35(1):2404718.
|
||
Epub 2024 Oct 13
|
||
doi: 10.1080/09546634.2024.2404718.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39396818" target="_blank">39396818</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38457930">Pentraxin 3 exacerbates psoriasiform dermatitis through regulation of macrophage polarization.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Liu J,
|
||
Qiu C,
|
||
Zhou Z,
|
||
Li J,
|
||
Zhen Y,
|
||
Wang R,
|
||
Zhuang Y,
|
||
Zhang F</span><br />
|
||
<span class="medgenPMjournal">Int Immunopharmacol</span>
|
||
2024 Mar 30;130:111805.
|
||
Epub 2024 Mar 7
|
||
doi: 10.1016/j.intimp.2024.111805.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38457930" target="_blank">38457930</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34405836">Systemic Treatment of Cutaneous Adverse Events After Immune Checkpoint Inhibitor Therapy: A Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Brown AM,
|
||
Masterson W,
|
||
Lo J,
|
||
Patel AB</span><br />
|
||
<span class="medgenPMjournal">Dermatitis</span>
|
||
2023 May-Jun;34(3):201-208.
|
||
Epub 2023 Jan 1
|
||
doi: 10.1097/DER.0000000000000776.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34405836" target="_blank">34405836</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31195782">Cutaneous effects of antihypertensive drugs.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Baccino D,
|
||
Merlo G,
|
||
Cozzani E,
|
||
Rosa GM,
|
||
Tini G,
|
||
Burlando M,
|
||
Parodi A</span><br />
|
||
<span class="medgenPMjournal">G Ital Dermatol Venereol</span>
|
||
2020 Apr;155(2):202-211.
|
||
Epub 2019 Jun 12
|
||
doi: 10.23736/S0392-0488.19.06360-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31195782" target="_blank">31195782</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26173479">Adiponectin regulates psoriasiform skin inflammation by suppressing IL-17 production from γδ-T cells.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shibata S,
|
||
Tada Y,
|
||
Hau CS,
|
||
Mitsui A,
|
||
Kamata M,
|
||
Asano Y,
|
||
Sugaya M,
|
||
Kadono T,
|
||
Masamoto Y,
|
||
Kurokawa M,
|
||
Yamauchi T,
|
||
Kubota N,
|
||
Kadowaki T,
|
||
Sato S</span><br />
|
||
<span class="medgenPMjournal">Nat Commun</span>
|
||
2015 Jul 15;6:7687.
|
||
doi: 10.1038/ncomms8687.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26173479" target="_blank">26173479</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Psoriasiform%20dermatitis%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 (40)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34863005">Ichthyosis, psoriasiform dermatitis, and recurrent fungal infections in patients with biallelic mutations in PERP.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Youssefian L,
|
||
Khodavaisy S,
|
||
Khosravi-Bachehmir F,
|
||
Park JS,
|
||
Saeidian AH,
|
||
Mahmoudi H,
|
||
Saffarian Z,
|
||
Naraghi ZS,
|
||
Kamyab-Hesari K,
|
||
Zeinali S,
|
||
Vahidnezhad H,
|
||
Uitto J</span><br />
|
||
<span class="medgenPMjournal">J Eur Acad Dermatol Venereol</span>
|
||
2022 Mar;36(3):472-479.
|
||
Epub 2021 Dec 29
|
||
doi: 10.1111/jdv.17856.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34863005" target="_blank">34863005</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33026774">Is TNF-α Inhibitor-Induced Psoriasiform Dermatitis Always Psoriasiform?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wei C,
|
||
Murphy EC,
|
||
Zahn J,
|
||
Friedman AJ</span><br />
|
||
<span class="medgenPMjournal">J Drugs Dermatol</span>
|
||
2020 Oct 1;19(10):1009-1010.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33026774" target="_blank">33026774</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28094165">Psoriasiform dermatitides: A brief review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wick MR</span><br />
|
||
<span class="medgenPMjournal">Semin Diagn Pathol</span>
|
||
2017 May;34(3):220-225.
|
||
Epub 2016 Dec 14
|
||
doi: 10.1053/j.semdp.2016.12.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28094165" target="_blank">28094165</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26173479">Adiponectin regulates psoriasiform skin inflammation by suppressing IL-17 production from γδ-T cells.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shibata S,
|
||
Tada Y,
|
||
Hau CS,
|
||
Mitsui A,
|
||
Kamata M,
|
||
Asano Y,
|
||
Sugaya M,
|
||
Kadono T,
|
||
Masamoto Y,
|
||
Kurokawa M,
|
||
Yamauchi T,
|
||
Kubota N,
|
||
Kadowaki T,
|
||
Sato S</span><br />
|
||
<span class="medgenPMjournal">Nat Commun</span>
|
||
2015 Jul 15;6:7687.
|
||
doi: 10.1038/ncomms8687.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26173479" target="_blank">26173479</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17456921">Blastomycosis-like pyoderma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sawalka SS,
|
||
Phiske MM,
|
||
Jerajani HR</span><br />
|
||
<span class="medgenPMjournal">Indian J Dermatol Venereol Leprol</span>
|
||
2007 Mar-Apr;73(2):117-9.
|
||
doi: 10.4103/0378-6323.31900.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17456921" target="_blank">17456921</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Psoriasiform%20dermatitis%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 (64)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39396818">Five-year real-world drug survival of dupilumab in severe atopic dermatitis and associate predictors.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Barei F,
|
||
Calzari P,
|
||
Valtellini L,
|
||
Chiei Gallo A,
|
||
Perego G,
|
||
Tavecchio S,
|
||
Zussino M,
|
||
Marzano AV,
|
||
Ferrucci S</span><br />
|
||
<span class="medgenPMjournal">J Dermatolog Treat</span>
|
||
2024 Dec;35(1):2404718.
|
||
Epub 2024 Oct 13
|
||
doi: 10.1080/09546634.2024.2404718.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39396818" target="_blank">39396818</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34704949">Two cases of psoriasiform dermatitis arising during dupilumab therapy and successfully treated with delgocitinib ointment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kurihara K,
|
||
Fujiyama T,
|
||
Tokura Y,
|
||
Honda T</span><br />
|
||
<span class="medgenPMjournal">Eur J Dermatol</span>
|
||
2021 Oct 1;31(5):658-660.
|
||
doi: 10.1684/ejd.2021.4140.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34704949" target="_blank">34704949</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33357345">Psoriasiform Dermatitis During Infliximab Therapy for Ulcerative Colitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Seiringer P,
|
||
Biedermann T,
|
||
Brockow K</span><br />
|
||
<span class="medgenPMjournal">Dtsch Arztebl Int</span>
|
||
2020 Sep 25;117(39):652.
|
||
doi: 10.3238/arztebl.2020.0652.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33357345" target="_blank">33357345</a><a href="/pmc/articles/PMC7829448" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33026774">Is TNF-α Inhibitor-Induced Psoriasiform Dermatitis Always Psoriasiform?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wei C,
|
||
Murphy EC,
|
||
Zahn J,
|
||
Friedman AJ</span><br />
|
||
<span class="medgenPMjournal">J Drugs Dermatol</span>
|
||
2020 Oct 1;19(10):1009-1010.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33026774" target="_blank">33026774</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28329474">Certolizumab-induced guttate psoriasiform dermatitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fischer R,
|
||
DaCunha M,
|
||
Rajpara A</span><br />
|
||
<span class="medgenPMjournal">Dermatol Online J</span>
|
||
2017 Jan 15;23(1)
|
||
<span class="bold">PMID: </span><a href="/pubmed/28329474" target="_blank">28329474</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Psoriasiform%20dermatitis%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 (94)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39396818">Five-year real-world drug survival of dupilumab in severe atopic dermatitis and associate predictors.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Barei F,
|
||
Calzari P,
|
||
Valtellini L,
|
||
Chiei Gallo A,
|
||
Perego G,
|
||
Tavecchio S,
|
||
Zussino M,
|
||
Marzano AV,
|
||
Ferrucci S</span><br />
|
||
<span class="medgenPMjournal">J Dermatolog Treat</span>
|
||
2024 Dec;35(1):2404718.
|
||
Epub 2024 Oct 13
|
||
doi: 10.1080/09546634.2024.2404718.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39396818" target="_blank">39396818</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/39161766">Case report: Psoriasiform eczema with immune-mediated comorbidities treated with upadacitinib.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Salvi I,
|
||
Parodi A,
|
||
Cozzani E,
|
||
Burlando M</span><br />
|
||
<span class="medgenPMjournal">Front Immunol</span>
|
||
2024;15:1432233.
|
||
Epub 2024 Aug 5
|
||
doi: 10.3389/fimmu.2024.1432233.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39161766" target="_blank">39161766</a><a href="/pmc/articles/PMC11330832" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38279614">Clinicopathological definition, management and prognostic value of mogamulizumab-associated rash and other cutaneous events: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Avallone G,
|
||
Roccuzzo G,
|
||
Pileri A,
|
||
Agostinelli C,
|
||
Maronese CA,
|
||
Aquino C,
|
||
Tavoletti G,
|
||
Onida F,
|
||
Fava P,
|
||
Ribero S,
|
||
Marzano AV,
|
||
Berti E,
|
||
Quaglino P,
|
||
Alberti-Violetti S</span><br />
|
||
<span class="medgenPMjournal">J Eur Acad Dermatol Venereol</span>
|
||
2024 Sep;38(9):1738-1748.
|
||
Epub 2024 Jan 26
|
||
doi: 10.1111/jdv.19801.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38279614" target="_blank">38279614</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30935778">GPR15 is not critically involved in the regulation of murine psoriasiform dermatitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sezin T,
|
||
Kempen L,
|
||
Meyne LM,
|
||
Mousavi S,
|
||
Zillikens D,
|
||
Sadik CD</span><br />
|
||
<span class="medgenPMjournal">J Dermatol Sci</span>
|
||
2019 Apr;94(1):196-204.
|
||
Epub 2019 Mar 12
|
||
doi: 10.1016/j.jdermsci.2019.01.008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30935778" target="_blank">30935778</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9436849">Netherton syndrome presenting as congenital psoriasis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shwayder T,
|
||
Banerjee S</span><br />
|
||
<span class="medgenPMjournal">Pediatr Dermatol</span>
|
||
1997 Nov-Dec;14(6):473-6.
|
||
doi: 10.1111/j.1525-1470.1997.tb00694.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9436849" target="_blank">9436849</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Psoriasiform%20dermatitis%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 (23)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38960840">Topical application of a BCL-2 inhibitor ameliorates imiquimod-induced psoriasiform dermatitis by eliminating senescent cells.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhu H,
|
||
Jiang J,
|
||
Yang M,
|
||
Zhao M,
|
||
He Z,
|
||
Tang C,
|
||
Song C,
|
||
Zhao M,
|
||
Akbar AN,
|
||
Reddy V,
|
||
Pan W,
|
||
Li S,
|
||
Tan Y,
|
||
Wu H,
|
||
Lu Q</span><br />
|
||
<span class="medgenPMjournal">J Dermatol Sci</span>
|
||
2024 Aug;115(2):54-63.
|
||
Epub 2024 Jun 18
|
||
doi: 10.1016/j.jdermsci.2024.06.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38960840" target="_blank">38960840</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38457930">Pentraxin 3 exacerbates psoriasiform dermatitis through regulation of macrophage polarization.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Liu J,
|
||
Qiu C,
|
||
Zhou Z,
|
||
Li J,
|
||
Zhen Y,
|
||
Wang R,
|
||
Zhuang Y,
|
||
Zhang F</span><br />
|
||
<span class="medgenPMjournal">Int Immunopharmacol</span>
|
||
2024 Mar 30;130:111805.
|
||
Epub 2024 Mar 7
|
||
doi: 10.1016/j.intimp.2024.111805.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38457930" target="_blank">38457930</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34707088">Inhibition of keratinocyte ferroptosis suppresses psoriatic inflammation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shou Y,
|
||
Yang L,
|
||
Yang Y,
|
||
Xu J</span><br />
|
||
<span class="medgenPMjournal">Cell Death Dis</span>
|
||
2021 Oct 27;12(11):1009.
|
||
doi: 10.1038/s41419-021-04284-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34707088" target="_blank">34707088</a><a href="/pmc/articles/PMC8551323" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27137868">Up-regulation of Interferon-inducible protein 16 contributes to psoriasis by modulating chemokine production in keratinocytes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cao T,
|
||
Shao S,
|
||
Li B,
|
||
Jin L,
|
||
Lei J,
|
||
Qiao H,
|
||
Wang G</span><br />
|
||
<span class="medgenPMjournal">Sci Rep</span>
|
||
2016 May 3;6:25381.
|
||
doi: 10.1038/srep25381.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27137868" target="_blank">27137868</a><a href="/pmc/articles/PMC4853747" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23918954">Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Augustin I,
|
||
Gross J,
|
||
Baumann D,
|
||
Korn C,
|
||
Kerr G,
|
||
Grigoryan T,
|
||
Mauch C,
|
||
Birchmeier W,
|
||
Boutros M</span><br />
|
||
<span class="medgenPMjournal">J Exp Med</span>
|
||
2013 Aug 26;210(9):1761-77.
|
||
Epub 2013 Aug 5
|
||
doi: 10.1084/jem.20121871.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23918954" target="_blank">23918954</a><a href="/pmc/articles/PMC3754868" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Psoriasiform%20dermatitis%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 (50)</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/38279614">Clinicopathological definition, management and prognostic value of mogamulizumab-associated rash and other cutaneous events: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Avallone G,
|
||
Roccuzzo G,
|
||
Pileri A,
|
||
Agostinelli C,
|
||
Maronese CA,
|
||
Aquino C,
|
||
Tavoletti G,
|
||
Onida F,
|
||
Fava P,
|
||
Ribero S,
|
||
Marzano AV,
|
||
Berti E,
|
||
Quaglino P,
|
||
Alberti-Violetti S</span><br />
|
||
<span class="medgenPMjournal">J Eur Acad Dermatol Venereol</span>
|
||
2024 Sep;38(9):1738-1748.
|
||
Epub 2024 Jan 26
|
||
doi: 10.1111/jdv.19801.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38279614" target="_blank">38279614</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35760771">Anti-tumour necrosis factor-induced skin rashes in inflammatory bowel disease: a systematic review and evidence-based management algorithm.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Au M,
|
||
Heddle G,
|
||
Young E,
|
||
Ryan E,
|
||
Graf S,
|
||
Tee D,
|
||
Philpott H</span><br />
|
||
<span class="medgenPMjournal">Intern Med J</span>
|
||
2023 Oct;53(10):1854-1865.
|
||
Epub 2022 Sep 30
|
||
doi: 10.1111/imj.15859.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35760771" target="_blank">35760771</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34423852">Dermoscopy, confocal microscopy and optical coherence tomography features of main inflammatory and autoimmune skin diseases: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Guida S,
|
||
Longhitano S,
|
||
Ardigò M,
|
||
Pampena R,
|
||
Ciardo S,
|
||
Bigi L,
|
||
Mandel VD,
|
||
Vaschieri C,
|
||
Manfredini M,
|
||
Pezzini C,
|
||
Arginelli F,
|
||
Farnetani F,
|
||
Zerbinati N,
|
||
Longo C,
|
||
Pellacani G</span><br />
|
||
<span class="medgenPMjournal">Australas J Dermatol</span>
|
||
2022 Feb;63(1):15-26.
|
||
Epub 2021 Aug 23
|
||
doi: 10.1111/ajd.13695.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34423852" target="_blank">34423852</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31195782">Cutaneous effects of antihypertensive drugs.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Baccino D,
|
||
Merlo G,
|
||
Cozzani E,
|
||
Rosa GM,
|
||
Tini G,
|
||
Burlando M,
|
||
Parodi A</span><br />
|
||
<span class="medgenPMjournal">G Ital Dermatol Venereol</span>
|
||
2020 Apr;155(2):202-211.
|
||
Epub 2019 Jun 12
|
||
doi: 10.23736/S0392-0488.19.06360-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31195782" target="_blank">31195782</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Psoriasiform%20dermatitis%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 (4)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
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|
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|
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|
||
</div>
|
||
<div class="supplemental col three_col last">
|
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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|
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Psoriasiform%20dermatitis" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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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=(%22psoriasiform%20dermatitis%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></ul></div>
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<a href="/pubmed?term=Psoriasiform%20dermatitis%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=2" target="_blank">Reviews in PubMed</a>
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<a class="brieflinkpopperctrl" href="/pmc?LinkName=medgen_pmc&from_uid=75508" ref="log$=recordlinks">PMC Articles</a>
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