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<!--
|
||
UID=57877
|
||
ConceptID=C0162285
|
||
-->
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||
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Palpebral edema</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>57877</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.">C0162285</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Pathologic Function</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Edema of eyelids; Puffy lids</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Edema of eyelid (89091004); Hydroblepharon (89091004)</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:0100540">HP:0100540</a></td></tr>
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|
||
<div class="portlet_content ln">Edema in the region of the eyelids. [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="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0162285[DISCUI]&test_type=Clinical" ref="ncbi_uid=57877">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">Palpebral edema</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/867442" ref="tree=MeSH" title="MedGen record for Abnormality of head or neck">Abnormality of head or neck</a></span><ul><li><span class="TLline"><a href="/medgen/867438" ref="tree=MeSH" title="MedGen record for Abnormality of the head">Abnormality of the head</a></span><ul><li><span class="TLline"><a href="/medgen/871375" ref="tree=MeSH" title="MedGen record for Abnormality of the face">Abnormality of the face</a></span><ul><li><span class="TLline"><a href="/medgen/871344" ref="tree=MeSH" title="MedGen record for Abnormality of the periorbital region">Abnormality of the periorbital region</a></span><ul><li><span class="TLline"><a href="/medgen/56223" ref="tree=MeSH" title="MedGen record for Periorbital edema">Periorbital edema</a></span><ul><li><span class="matched_ds">Palpebral edema</span><ul><li><span class="TLline"><a href="/medgen/14154" ref="tree=MeSH" title="MedGen record for Blepharochalasis">Blepharochalasis</a></span></li><li><span class="TLline"><a href="/medgen/825842" ref="tree=MeSH" title="MedGen record for Lower eyelid edema">Lower eyelid edema</a></span></li><li><span class="TLline"><a href="/medgen/825252" ref="tree=MeSH" title="MedGen record for Upper eyelid edema">Upper eyelid edema</a></span></li></ul></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">
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||
<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>
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<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_83284"><div><strong>Reis-Bucklers corneal dystrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>83284</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.">C0339278</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Reis-Bucklers corneal dystrophy (CDRB) is an autosomal dominant disorder of the superficial corneal stroma that manifests as recurrent corneal erosions in early childhood. Affected individuals develop corneal opacities that result in significant visual impairment. Microscopically, CDRB may be differentiated from other forms of corneal dystrophy by confluent opacities in the Bowman layer and subepithelium, which are the product of extracellular bodies that stain red with Masson trichrome stain and appear as crystalloid rod-shaped bodies on transmission electron microscopy (summary by Tanhehco et al., 2006).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/83284">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_375070"><div><strong>Hypotrichosis-lymphedema-telangiectasia syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>375070</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.">C1843004</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hypotrichosis-lymphedema-telangiectasia syndrome is an autosomal recessive disorder characterized by these 3 features, which begin at birth or in early childhood and are progressive (summary by Irrthum et al., 2003).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/375070">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_340355"><div><strong>Congenital pulmonary lymphangiectasia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>340355</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.">C1849554</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Pulmonary lymphangiectasia is a rare congenital vascular dysplasia characterized by an increased number of dilated pulmonary lymphatics in the subpleural, peribronchial, and interlobular septa. Respiratory distress is usually noted immediately after birth (summary by Stevenson et al., 2006).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/340355">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_339994"><div><strong>Phelan-McDermid syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>339994</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.">C1853490</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Phelan-McDermid syndrome-SHANK3 related (PMS-SHANK3 related) is characterized by neonatal hypotonia, absent to severely delayed speech, developmental delay, and minor dysmorphic facial features. Most affected individuals have moderate-to-profound intellectual disability. Other features include relatively large fleshy hands, dysplastic toenails, and decreased perspiration that results in a tendency to overheat. Normal stature and normal head size distinguish PMS-SHANK3 related from other autosomal chromosome disorders. Neurobehavioral characteristics include mouthing or chewing non-food items, decreased perception of pain, and autism spectrum disorder or autistic-like affect and behavior. Some individuals experience regression / loss of skills, epilepsy, ataxic/abnormal gait, and sleep disturbance (difficulty falling asleep and staying asleep, hypersomnia, and parasomnias). Less commonly, affected individuals may have strabismus, vision problems (hyperopia or myopia), cardiac anomalies, renal anomalies, and lymphedema. Those who have PMS-SHANK3 related due to a ring chromosome 22 also have a high risk of developing features of NF2-related schwannomatosis (NF2).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/339994">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_357183"><div><strong>Scalp-ear-nipple syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>357183</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.">C1867020</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Scalp-ear-nipple syndrome is characterized by aplasia cutis congenita of the scalp, breast anomalies that range from hypothelia or athelia to amastia, and minor anomalies of the external ears. Less frequent clinical characteristics include nail dystrophy, dental anomalies, cutaneous syndactyly of the digits, and renal malformations. Penetrance appears to be high, although there is substantial variable expressivity within families (Marneros et al., 2013).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/357183">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_435914"><div><strong>Mucolipidosis type II</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>435914</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.">C2673377</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">GNPTAB-related disorders comprise the phenotypes mucolipidosis II (ML II) and mucolipidosis IIIa/ß (ML IIIa/ß), and phenotypes intermediate between ML II and ML IIIa/ß. ML II is evident at birth and slowly progressive; death most often occurs in early childhood. Orthopedic abnormalities present at birth may include thoracic deformity, kyphosis, clubfeet, deformed long bones, and/or dislocation of the hip(s). Growth often ceases in the second year of life; contractures develop in all large joints. The skin is thickened, facial features are coarse, and gingiva are hypertrophic. All children have cardiac involvement, most commonly thickening and insufficiency of the mitral valve and, less frequently, the aortic valve. Progressive mucosal thickening narrows the airways, and gradual stiffening of the thoracic cage contributes to respiratory insufficiency, the most common cause of death. ML IIIa/ß becomes evident at about age three years with slow growth rate and short stature; joint stiffness and pain initially in the shoulders, hips, and fingers; gradual mild coarsening of facial features; and normal to mildly impaired cognitive development. Pain from osteoporosis becomes more severe during adolescence. Cardiorespiratory complications (restrictive lung disease, thickening and insufficiency of the mitral and aortic valves, left and/or right ventricular hypertrophy) are common causes of death, typically in early to middle adulthood. Phenotypes intermediate between ML II and ML IIIa/ß are characterized by physical growth in infancy that resembles that of ML II and neuromotor and speech development that resemble that of ML IIIa/ß.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/435914">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_416526"><div><strong>RIN2 syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>416526</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.">C2751321</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">MACS syndrome is an autosomal recessive connective tissue disorder named for the variable features of macrocephaly, alopecia, cutis laxa, and scoliosis (summary by Kameli et al., 2020).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/416526">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_763187"><div><strong>Peroxisome biogenesis disorder 2A (Zellweger)</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>763187</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.">C3550273</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The peroxisome biogenesis disorder (PBD) Zellweger syndrome (ZS) is an autosomal recessive multiple congenital anomaly syndrome. Affected children present in the newborn period with profound hypotonia, seizures, and inability to feed. Characteristic craniofacial anomalies, eye abnormalities, neuronal migration defects, hepatomegaly, and chondrodysplasia punctata are present. Children with this condition do not show any significant development and usually die in the first year of life (summary by Steinberg et al., 2006). For a complete phenotypic description and a discussion of genetic heterogeneity of Zellweger syndrome, see 214100. Individuals with PBDs of complementation group 2 (CG2) have mutations in the PEX5 gene. For information on the history of PBD complementation groups, see 214100.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/763187">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_766575"><div><strong>Cerebellar dysfunction with variable cognitive and behavioral abnormalities</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>766575</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.">C3553661</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Cerebellar dysfunction with variable cognitive and behavioral abnormalities (CECBA) is an autosomal dominant neurologic disorder with significant phenotypic heterogeneity, even within families. The disorder is most often diagnosed through genetic analysis with retrospective clinical phenotyping. Symptom onset is usually in early childhood, although later onset, even in adulthood, has been reported. Most affected individuals show global developmental delay from early childhood, particularly of motor and language skills. Many have mild intellectual disability; behavioral and psychiatric abnormalities such as autism and obsessive-compulsive disorder are also often observed. The movement disorder is prominent and may include cerebellar signs such as ataxia, tremor, dysmetria, poor coordination, and dysarthria. Other abnormal movements including spasticity, myoclonus, and dystonia have been reported, thus widening the phenotypic spectrum. Brain imaging is usually normal, but may show cerebellar atrophy or nonspecific white matter lesions. Variable dysmorphic facial features may also be present (summary by Thevenon et al., 2012; Jacobs et al., 2021; Wijnen et al., 2020).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/766575">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_766854"><div><strong>Peroxisome biogenesis disorder 5A (Zellweger)</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>766854</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.">C3553940</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The peroxisomal biogenesis disorder (PBD) Zellweger syndrome (ZS) is an autosomal recessive multiple congenital anomaly syndrome. Affected children present in the newborn period with profound hypotonia, seizures, and inability to feed. Characteristic craniofacial anomalies, eye abnormalities, neuronal migration defects, hepatomegaly, and chondrodysplasia punctata are present. Children with this condition do not show any significant development and usually die in the first year of life (summary by Steinberg et al., 2006). For a complete phenotypic description and a discussion of genetic heterogeneity of Zellweger syndrome, see 214100. Individuals with PBDs of complementation group 5 (CG5, equivalent to CG10 and CGF) have mutations in the PEX2 gene. For information on the history of PBD complementation groups, see 214100.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/766854">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1373459"><div><strong>Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1373459</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.">C4317151</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome is an autosomal dominant disorder characterized by these 4 features, which begin in early childhood and are progressive (summary by Moalem et al., 2015).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1373459">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1794167"><div><strong>Developmental delay, impaired speech, and behavioral abnormalities</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1794167</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.">C5561957</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Developmental delay, impaired speech, and behavioral abnormalities (DDISBA) is characterized by global developmental delay apparent from early childhood. Intellectual disability can range from mild to severe. Additional variable features may include dysmorphic facial features, seizures, hypotonia, motor abnormalities such as Tourette syndrome or dystonia, and hearing loss (summary by Cousin et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1794167">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_766575" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cerebellar dysfunction with variable cognitive and behavioral abnormalities</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_340355" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Congenital pulmonary lymphangiectasia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1794167" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Developmental delay, impaired speech, and behavioral abnormalities</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_375070" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypotrichosis-lymphedema-telangiectasia syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1373459" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (12)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_435914" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mucolipidosis type II</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_763187" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Peroxisome biogenesis disorder 2A (Zellweger)</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_766854" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Peroxisome biogenesis disorder 5A (Zellweger)</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_339994" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Phelan-McDermid syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_83284" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Reis-Bucklers corneal dystrophy</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_416526" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">RIN2 syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_357183" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Scalp-ear-nipple 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>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36283416">The Management of Chemosis after Blepharoplasty.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ní Dhubhghaill S,
|
||
Faris C</span><br />
|
||
<span class="medgenPMjournal">Facial Plast Surg</span>
|
||
2023 Feb;39(1):53-56.
|
||
Epub 2022 Oct 25
|
||
doi: 10.1055/a-1967-6050.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36283416" target="_blank">36283416</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26176369">Differential Diagnosis of the Swollen Red Eyelid.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Carlisle RT,
|
||
Digiovanni J</span><br />
|
||
<span class="medgenPMjournal">Am Fam Physician</span>
|
||
2015 Jul 15;92(2):106-12.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26176369" target="_blank">26176369</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23744974">Management of postblepharoplasty chemosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McCord CD,
|
||
Kreymerman P,
|
||
Nahai F,
|
||
Walrath JD</span><br />
|
||
<span class="medgenPMjournal">Aesthet Surg J</span>
|
||
2013 Jul;33(5):654-61.
|
||
Epub 2013 Jun 6
|
||
doi: 10.1177/1090820X13487016.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23744974" target="_blank">23744974</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(palpebral%20edema)%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 (37)</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/37526456">Infectious Mononucleosis: An Updated Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Leung AKC,
|
||
Lam JM,
|
||
Barankin B</span><br />
|
||
<span class="medgenPMjournal">Curr Pediatr Rev</span>
|
||
2024;20(3):305-322.
|
||
doi: 10.2174/1573396320666230801091558.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37526456" target="_blank">37526456</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38097988">New daily persistent headache after SARS-CoV-2 infection in Latin America: a cross-sectional study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Carrión-Nessi FS,
|
||
Ascanio LC,
|
||
Pineda-Arapé AG,
|
||
Omaña-Ávila ÓD,
|
||
Mendoza-Millán DL,
|
||
Romero SR,
|
||
Almao-Rivero AB,
|
||
Camejo-Ávila NA,
|
||
Gebran-Chedid KJ,
|
||
Rodriguez-Saavedra CM,
|
||
Freitas-De Nobrega DC,
|
||
Castañeda SA,
|
||
Forero-Peña JL,
|
||
Delgado-Noguera LA,
|
||
Meneses-Ramírez LK,
|
||
Cotuá JC,
|
||
Rodriguez-Morales AJ,
|
||
Forero-Peña DA,
|
||
Paniz-Mondolfi AE</span><br />
|
||
<span class="medgenPMjournal">BMC Infect Dis</span>
|
||
2023 Dec 14;23(1):877.
|
||
doi: 10.1186/s12879-023-08898-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38097988" target="_blank">38097988</a><a href="/pmc/articles/PMC10722794" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28690724">Imaging of complicated frontal sinusitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kolsi N,
|
||
Zrig A,
|
||
Chouchène H,
|
||
Bouatay R,
|
||
Harrathi K,
|
||
Koubaa J</span><br />
|
||
<span class="medgenPMjournal">Pan Afr Med J</span>
|
||
2017;26:209.
|
||
Epub 2017 Apr 19
|
||
doi: 10.11604/pamj.2017.26.209.11817.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28690724" target="_blank">28690724</a><a href="/pmc/articles/PMC5491736" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25185371">Post-marketing safety monitoring of shenqifuzheng injection: a solution made of dangshen (Radix Codonopsis) and huangqi (Radix Astragali Mongolici).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ai Q,
|
||
Zhang W,
|
||
Xie Y,
|
||
Huang W,
|
||
Liang H,
|
||
Cao H</span><br />
|
||
<span class="medgenPMjournal">J Tradit Chin Med</span>
|
||
2014 Aug;34(4):498-503.
|
||
doi: 10.1016/s0254-6272(15)30053-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25185371" target="_blank">25185371</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15456948">Ocular metastases from breast carcinoma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mejía-Novelo A,
|
||
Alvarado-Miranda A,
|
||
Morales-Vázquez F,
|
||
Gamboa-Vignole C,
|
||
Núñez-Gómez R,
|
||
Castañeda-Soto N,
|
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Dueñas-González A,
|
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Candelaria-Hernández M,
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Lara-Medina F</span><br />
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<span class="medgenPMjournal">Med Oncol</span>
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2004;21(3):217-21.
|
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doi: 10.1385/MO:21:3:217.
|
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<span class="bold">PMID: </span><a href="/pubmed/15456948" target="_blank">15456948</a></div>
|
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Palpebral%20edema%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 (15)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37526456">Infectious Mononucleosis: An Updated Review.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Leung AKC,
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Lam JM,
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Barankin B</span><br />
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<span class="medgenPMjournal">Curr Pediatr Rev</span>
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2024;20(3):305-322.
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doi: 10.2174/1573396320666230801091558.
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<span class="bold">PMID: </span><a href="/pubmed/37526456" target="_blank">37526456</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Bonito FJP,
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Cerejeira D,
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Cunha H</span><br />
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2020 Jan;37(1):211-212.
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<span class="bold">PMID: </span><a href="/pubmed/31997442" target="_blank">31997442</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/29057745">Palpebral Edema and Eosinophilia.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Méndez Alcalde JD,
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Cabrerizo Ballesteros S,
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García Villamuza Y</span><br />
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<div class="nl"><a target="_blank" href="/pubmed/25973075">Crescentic acute glomerulonephritis with isolated C3 deposition: a case report and review of literature.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Mao S,
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<div class="nl"><a target="_blank" href="/pubmed/16327570">Parry-Romberg syndrome.</a></div>
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Leonardi A,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Palpebral%20edema%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 (37)</a></div><h3 class="subhead">Therapy</h3>
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<div class="nl"><a target="_blank" href="/pubmed/30376464">Cutaneous adverse event associated with vemurafenib in a 3-year-old pediatric patient with BRAF mutation-positive metastatic melanoma and factor X deficiency.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Büyükkapu Bay S,
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Kebudi R,
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Zülfikar B</span><br />
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<span class="medgenPMjournal">Melanoma Res</span>
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2019 Feb;29(1):99-101.
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doi: 10.1097/CMR.0000000000000537.
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<span class="bold">PMID: </span><a href="/pubmed/30376464" target="_blank">30376464</a></div>
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||
<div class="nl"><a target="_blank" href="/pubmed/29057745">Palpebral Edema and Eosinophilia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Méndez Alcalde JD,
|
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Cabrerizo Ballesteros S,
|
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García Villamuza Y</span><br />
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<span class="medgenPMjournal">J Investig Allergol Clin Immunol</span>
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2017;27(5):330-331.
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doi: 10.18176/jiaci.0183.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29057745" target="_blank">29057745</a></div>
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||
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||
<div class="nl"><a target="_blank" href="/pubmed/25973075">Crescentic acute glomerulonephritis with isolated C3 deposition: a case report and review of literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mao S,
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Xuan X,
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Sha Y,
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Zhao S,
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Zhang A,
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Huang S</span><br />
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<span class="medgenPMjournal">Int J Clin Exp Pathol</span>
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2015;8(2):1826-9.
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Epub 2015 Feb 1
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<span class="bold">PMID: </span><a href="/pubmed/25973075" target="_blank">25973075</a><a href="/pmc/articles/PMC4396300" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
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|
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<div class="nl"><a target="_blank" href="/pubmed/25185371">Post-marketing safety monitoring of shenqifuzheng injection: a solution made of dangshen (Radix Codonopsis) and huangqi (Radix Astragali Mongolici).</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Ai Q,
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Zhang W,
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Xie Y,
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Huang W,
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Liang H,
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Cao H</span><br />
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<span class="medgenPMjournal">J Tradit Chin Med</span>
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doi: 10.1016/s0254-6272(15)30053-4.
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<span class="bold">PMID: </span><a href="/pubmed/25185371" target="_blank">25185371</a></div>
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||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25171844">Post vaccine acute disseminated encephalomyelitis as the first manifestation of chromosome 22q11.2 deletion syndrome in a 15-month old baby: a case report.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Valenzise M,
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Cascio A,
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Wasniewska M,
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Zirilli G,
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Catena MA,
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Arasi S</span><br />
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<span class="medgenPMjournal">Vaccine</span>
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2014 Sep 29;32(43):5552-4.
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Epub 2014 Aug 30
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doi: 10.1016/j.vaccine.2014.08.047.
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<span class="bold">PMID: </span><a href="/pubmed/25171844" target="_blank">25171844</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Palpebral%20edema%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 (18)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/30376464">Cutaneous adverse event associated with vemurafenib in a 3-year-old pediatric patient with BRAF mutation-positive metastatic melanoma and factor X deficiency.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Büyükkapu Bay S,
|
||
Kebudi R,
|
||
Zülfikar B</span><br />
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<span class="medgenPMjournal">Melanoma Res</span>
|
||
2019 Feb;29(1):99-101.
|
||
doi: 10.1097/CMR.0000000000000537.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30376464" target="_blank">30376464</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25973075">Crescentic acute glomerulonephritis with isolated C3 deposition: a case report and review of literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mao S,
|
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Xuan X,
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Sha Y,
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Zhao S,
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Zhang A,
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Huang S</span><br />
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<span class="medgenPMjournal">Int J Clin Exp Pathol</span>
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2015;8(2):1826-9.
|
||
Epub 2015 Feb 1
|
||
<span class="bold">PMID: </span><a href="/pubmed/25973075" target="_blank">25973075</a><a href="/pmc/articles/PMC4396300" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25185371">Post-marketing safety monitoring of shenqifuzheng injection: a solution made of dangshen (Radix Codonopsis) and huangqi (Radix Astragali Mongolici).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ai Q,
|
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Zhang W,
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Xie Y,
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Huang W,
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Liang H,
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Cao H</span><br />
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<span class="medgenPMjournal">J Tradit Chin Med</span>
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2014 Aug;34(4):498-503.
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doi: 10.1016/s0254-6272(15)30053-4.
|
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<span class="bold">PMID: </span><a href="/pubmed/25185371" target="_blank">25185371</a></div>
|
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||
<div class="nl"><a target="_blank" href="/pubmed/15456948">Ocular metastases from breast carcinoma.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Mejía-Novelo A,
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Alvarado-Miranda A,
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Morales-Vázquez F,
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Gamboa-Vignole C,
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Núñez-Gómez R,
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Castañeda-Soto N,
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Dueñas-González A,
|
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Candelaria-Hernández M,
|
||
Lara-Medina F</span><br />
|
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<span class="medgenPMjournal">Med Oncol</span>
|
||
2004;21(3):217-21.
|
||
doi: 10.1385/MO:21:3:217.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15456948" target="_blank">15456948</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2093719">Long-term follow-up of a child with idiopathic restrictive cardiomyopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Miyazaki A,
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Ichida F,
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Suzuki Y,
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Okada T</span><br />
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<span class="bold">PMID: </span><a href="/pubmed/2093719" target="_blank">2093719</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Palpebral%20edema%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 (14)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37526456">Infectious Mononucleosis: An Updated Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Leung AKC,
|
||
Lam JM,
|
||
Barankin B</span><br />
|
||
<span class="medgenPMjournal">Curr Pediatr Rev</span>
|
||
2024;20(3):305-322.
|
||
doi: 10.2174/1573396320666230801091558.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37526456" target="_blank">37526456</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32481733">Pitt-Hopkins Syndrome: Clinical and Molecular Findings of a 5-Year-Old Patient.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tripon F,
|
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Bogliș A,
|
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Micheu C,
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Streață I,
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Bănescu C</span><br />
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<span class="medgenPMjournal">Genes (Basel)</span>
|
||
2020 May 28;11(6)
|
||
doi: 10.3390/genes11060596.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32481733" target="_blank">32481733</a><a href="/pmc/articles/PMC7349262" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30376464">Cutaneous adverse event associated with vemurafenib in a 3-year-old pediatric patient with BRAF mutation-positive metastatic melanoma and factor X deficiency.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Büyükkapu Bay S,
|
||
Kebudi R,
|
||
Zülfikar B</span><br />
|
||
<span class="medgenPMjournal">Melanoma Res</span>
|
||
2019 Feb;29(1):99-101.
|
||
doi: 10.1097/CMR.0000000000000537.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30376464" target="_blank">30376464</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30321516">Reconstruction of Full-Thickness Lower Lid Defects Using Texier's Procedure: Retrospective Assessment of the Indications.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cristofari S,
|
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Rem K,
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Revol M,
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Atlan M,
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Stivala A</span><br />
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<span class="medgenPMjournal">J Oral Maxillofac Surg</span>
|
||
2019 Feb;77(2):433-439.
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||
Epub 2018 Sep 20
|
||
doi: 10.1016/j.joms.2018.09.007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30321516" target="_blank">30321516</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25185371">Post-marketing safety monitoring of shenqifuzheng injection: a solution made of dangshen (Radix Codonopsis) and huangqi (Radix Astragali Mongolici).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ai Q,
|
||
Zhang W,
|
||
Xie Y,
|
||
Huang W,
|
||
Liang H,
|
||
Cao H</span><br />
|
||
<span class="medgenPMjournal">J Tradit Chin Med</span>
|
||
2014 Aug;34(4):498-503.
|
||
doi: 10.1016/s0254-6272(15)30053-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25185371" target="_blank">25185371</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Palpebral%20edema%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 (10)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
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|
||
<div class=" bottom">
|
||
|
||
</div>
|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
||
<!-- MedGen supplemental column starts here -->
|
||
<div class="rightCol mgCol">
|
||
<div class="portlet mgSection" id="ID_113">
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul id="my-toc"></ul></div>
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<div class="portlet mgSection" id="ID_106">
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Genetic_Testing_Registry">Genetic Testing Registry</h1><a sid="106" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C0162285%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (8)</a></li>
|
||
<li><a href="/gtr/tests?term=C0162285%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (8)</a></li>
|
||
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C0162285%5bDISCUI%5d" target="_blank">See all (8)</a></total></li>
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</ul></div>
|
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</div>
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_resources">Clinical resources</h1><a sid="119" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Palpebral%20edema" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
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</div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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