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<meta name="keywords" content="C0423276, ac shallow, finding, shallow ac, shallow anterior chamber, shallow anterior chamber of eye, shallow anterior chambers, slitlike anterior chamber angles in children, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="Reduced depth of the anterior chamber, i.e., the anteroposterior distance between the cornea and the iris is decreased." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=602215
|
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ConceptID=C0423276
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Shallow anterior chamber</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>602215</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.">C0423276</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding; Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Slitlike anterior chamber angles in children</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Shallow AC (246986004); AC shallow (246986004); Shallow anterior chamber of eye (246986004)</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:0000594">HP:0000594</a></td></tr>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">Reduced depth of the anterior chamber, i.e., the anteroposterior distance between the cornea and the iris is decreased. [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 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=C0423276[DISCUI]&test_type=Clinical" ref="ncbi_uid=602215">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">Shallow anterior chamber</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/1370071" ref="tree=MeSH" title="MedGen record for Abnormality of the eye">Abnormality of the eye</a></span><ul><li><span class="TLline"><a href="/medgen/868526" ref="tree=MeSH" title="MedGen record for Abnormal eye morphology">Abnormal eye morphology</a></span><ul><li><span class="TLline"><a href="/medgen/870894" ref="tree=MeSH" title="MedGen record for Abnormal anterior eye segment morphology">Abnormal anterior eye segment morphology</a></span><ul><li><span class="TLline"><a href="/medgen/463532" ref="tree=MeSH" title="MedGen record for Abnormal anterior chamber morphology">Abnormal anterior chamber morphology</a></span><ul><li><span class="matched_ds">Shallow anterior chamber</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_112">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_75615"><div><strong>Atrophia bulborum hereditaria</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75615</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.">C0266526</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Norrie disease (ND) is an X-linked recessive disorder characterized by very early childhood blindness due to degenerative and proliferative changes of the neuroretina. Approximately 50% of patients show some form of progressive mental disorder, often with psychotic features, and about one-third of patients develop sensorineural deafness in the second decade. In addition, some patients have more complex phenotypes, including growth failure and seizures (Berger et al., 1992). Warburg (1966) noted confusion of the terms 'pseudoglioma' and microphthalmia with Norrie disease in the literature. 'Pseudoglioma' is a nonspecific term for any condition resembling retinoblastoma and can have diverse causes, including inflammation, hemorrhage, trauma, neoplasia, or congenital malformation, and often shows unilateral involvement. Thus, 'pseudoglioma' is not an acceptable clinical or pathologic diagnosis (see Duke, 1958).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/75615">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_98034"><div><strong>GAPO syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>98034</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.">C0406723</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">GAPO syndrome is the acronymic designation for a complex of growth retardation, alopecia, pseudoanodontia (failure of tooth eruption), and progressive optic atrophy (Tipton and Gorlin, 1984). Ilker et al. (1999) and Bayram et al. (2014) noted that optic atrophy is not a consistent feature of the disorder.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/98034">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_330396"><div><strong>Facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>330396</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.">C1832167</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Traboulsi syndrome is characterized by dislocated crystalline lenses and anterior segment abnormalities in association with a distinctive facies involving flat cheeks and a beaked nose. Some affected individuals develop highly unusual nontraumatic conjunctival cysts (filtering blebs), presumably caused by abnormal thinning of the sclera (Patel et al., 2014).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/330396">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_337030"><div><strong>Exudative vitreoretinopathy 2, X-linked</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>337030</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.">C1844579</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Familial exudative vitreoretinopathy (FEVR) is an inherited disorder characterized by the incomplete development of the retinal vasculature. Its clinical appearance varies considerably, even within families, with severely affected patients often registered as blind during infancy, whereas mildly affected patients with few or no visual problems may have such a small area of avascularity in their peripheral retina that it is visible only by fluorescein angiography. It is believed that this peripheral avascularity is the primary anomaly in FEVR and results from defective retinal angiogenesis. The sight-threatening features of the FEVR phenotype are considered secondary to retinal avascularity and develop because of the resulting retinal ischemia; they include the development of hyperpermeable blood vessels, neovascularization, vitreoretinal traction, retinal folds, and retinal detachments (summary by Poulter et al., 2010). For a discussion of genetic heterogeneity of FEVR, see EVR1 (133780).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/337030">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_400728"><div><strong>Colobomatous macrophthalmia-microcornea syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>400728</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.">C1865286</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Colobomatous macrophthalmia with microcornea (MACOM) is an autosomal dominant eye malformation characterized by microcornea with increased axial length, coloboma of the iris and optic disc, and severe myopia (summary by Beleggia et al., 2015).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/400728">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_358388"><div><strong>Weill-Marchesani syndrome 2, dominant</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>358388</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.">C1869115</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Weill-Marchesani syndrome (WMS) is a connective tissue disorder characterized by abnormalities of the lens of the eye, short stature, brachydactyly, joint stiffness, and cardiovascular defects. The ocular problems, typically recognized in childhood, include microspherophakia (small spherical lens), myopia secondary to the abnormal shape of the lens, ectopia lentis (abnormal position of the lens), and glaucoma, which can lead to blindness. Height of adult males is 142-169 cm; height of adult females is 130-157 cm. Autosomal recessive WMS cannot be distinguished from autosomal dominant WMS by clinical findings alone.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/358388">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_370100"><div><strong>Persistent hyperplastic primary vitreous, autosomal recessive</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>370100</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C1969783</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Persistent hyperplastic primary vitreous (PHPV), also termed 'persistent fetal vasculature,' is a developmental malformation of the eye in which the primary vitreous fails to regress in utero, resulting in the presence of a retrolental fibrovascular membrane with persistence of the posterior portion of the tunica vasculosa lentis and hyaloid artery. This abnormality is usually unilateral and associated with microphthalmia, cataract, glaucoma, and congenital retinal nonattachment (see Haddad et al., 1978; Khaliq et al., 2001; Prasov et al., 2012). PHPV shares phenotypic overlap with Norrie disease (310600). Genetic Heterogeneity of Persistent Hyperplastic Primary Vitreous A dominant form of PHPV has been described (PHPVAD; 611308).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/370100">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_412872"><div><strong>Exudative vitreoretinopathy 5</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>412872</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.">C2750079</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Familial exudative vitreoretinopathy is an inherited blinding disorder caused by defects in the development of retinal vasculature. There is extensive variation in disease severity among patients, even between members of the same family. Severely affected individuals often are registered as blind during infancy and can present with a phenotype resembling retinal dysplasia. Conversely, mildly affected individuals frequently have few or no visual problems and may have just a small area of avascularity in their peripheral retina, detectable only by fluorescein angiography (summary by Poulter et al., 2012). For a discussion of genetic heterogeneity of familial exudative vitreoretinopathy (FEVR), see EVR1 (133780).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/412872">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_416383"><div><strong>Weill-Marchesani 4 syndrome, recessive</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>416383</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information."><span class="highlight" style="background-color:">C2750787</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Weill-Marchesani syndrome (WMS) is a connective tissue disorder characterized by abnormalities of the lens of the eye, short stature, brachydactyly, joint stiffness, and cardiovascular defects. The ocular problems, typically recognized in childhood, include microspherophakia (small spherical lens), myopia secondary to the abnormal shape of the lens, ectopia lentis (abnormal position of the lens), and glaucoma, which can lead to blindness. Height of adult males is 142-169 cm; height of adult females is 130-157 cm. Autosomal recessive WMS cannot be distinguished from autosomal dominant WMS by clinical findings alone.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/416383">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_444153"><div><strong>Retinal degeneration-nanophthalmos-glaucoma syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>444153</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.">C2931831</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Syndrome with characteristics of progressive pigmentary retinal degeneration (with nyctalopia and visual field restriction), cystic macular degeneration and angle closure glaucoma. It has been described in seven members of one family. Patients also have hyperopia and nanophthalmos. The mode of transmission is autosomal recessive.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/444153">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_481833"><div><strong>Warburg micro syndrome 3</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>481833</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.">C3280203</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">RAB18 deficiency is the molecular deficit underlying both Warburg micro syndrome (characterized by eye, nervous system, and endocrine abnormalities) and Martsolf syndrome (characterized by similar – but milder – findings). To date Warburg micro syndrome comprises >96% of reported individuals with genetically defined RAB18 deficiency. The hallmark ophthalmologic findings are bilateral congenital cataracts, usually accompanied by microphthalmia, microcornea (diameter <10), and small atonic pupils. Poor vision despite early cataract surgery likely results from progressive optic atrophy and cortical visual impairment. Individuals with Warburg micro syndrome have severe to profound intellectual disability (ID); those with Martsolf syndrome have mild to moderate ID. Some individuals with RAB18 deficiency also have epilepsy. In Warburg micro syndrome, a progressive ascending spastic paraplegia typically begins with spastic diplegia and contractures during the first year, followed by upper-limb involvement leading to spastic quadriplegia after about age five years, often eventually causing breathing difficulties. In Martsolf syndrome infantile hypotonia is followed primarily by slowly progressive lower-limb spasticity. Hypogonadism – when present – manifests in both syndromes, in males as micropenis and/or cryptorchidism and in females as hypoplastic labia minora, clitoral hypoplasia, and small introitus.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/481833">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_762106"><div><strong>Ectopia lentis 1, isolated, autosomal dominant</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>762106</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.">C3541518</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Ectopia lentis is defined as an abnormal stretching of the zonular fibers that leads to lens dislocation, resulting in acute or chronic visual impairment (Greene et al., 2010). Citing the revised Ghent criteria for Marfan syndrome, Loeys et al. (2010) proposed the designation 'ectopia lentis syndrome' (ELS) for patients with ectopia lentis and a mutation in the FBN1 gene who lack aortic involvement, to highlight the systemic nature of the condition and to emphasize the need for assessment of features outside the ocular system (see DIAGNOSIS). Genetic Heterogeneity of Isolated Ectopia Lentis An autosomal recessive form of isolated ectopia lentis (ECTOL2; 225100) is caused by mutation in the ADAMTSL4 gene (610113).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/762106">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_766699"><div><strong>Weill-Marchesani syndrome 3</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>766699</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.">C3553785</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Weill-Marchesani syndrome (WMS) is a connective tissue disorder characterized by abnormalities of the lens of the eye, short stature, brachydactyly, joint stiffness, and cardiovascular defects. The ocular problems, typically recognized in childhood, include microspherophakia (small spherical lens), myopia secondary to the abnormal shape of the lens, ectopia lentis (abnormal position of the lens), and glaucoma, which can lead to blindness. Height of adult males is 142-169 cm; height of adult females is 130-157 cm. Autosomal recessive WMS cannot be distinguished from autosomal dominant WMS by clinical findings alone.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/766699">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1637058"><div><strong>Weill-Marchesani syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1637058</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.">C4552002</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Weill-Marchesani syndrome (WMS) is a connective tissue disorder characterized by abnormalities of the lens of the eye, short stature, brachydactyly, joint stiffness, and cardiovascular defects. The ocular problems, typically recognized in childhood, include microspherophakia (small spherical lens), myopia secondary to the abnormal shape of the lens, ectopia lentis (abnormal position of the lens), and glaucoma, which can lead to blindness. Height of adult males is 142-169 cm; height of adult females is 130-157 cm. Autosomal recessive WMS cannot be distinguished from autosomal dominant WMS by clinical findings alone.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1637058">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_75615" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Atrophia bulborum hereditaria</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_400728" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Colobomatous macrophthalmia-microcornea syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_762106" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Ectopia lentis 1, isolated, autosomal dominant</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_337030" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Exudative vitreoretinopathy 2, X-linked</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_412872" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Exudative vitreoretinopathy 5</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (14)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_330396" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_98034" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">GAPO syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_370100" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Persistent hyperplastic primary vitreous, autosomal recessive</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_444153" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Retinal degeneration-nanophthalmos-glaucoma syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_481833" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Warburg micro syndrome 3</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_416383" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Weill-Marchesani 4 syndrome, recessive</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1637058" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Weill-Marchesani syndrome 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_358388" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Weill-Marchesani syndrome 2, dominant</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_766699" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Weill-Marchesani syndrome 3</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/26518079">New findings in the diagnosis and treatment of primary angle-closure glaucoma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Marchini G,
|
||
Chemello F,
|
||
Berzaghi D,
|
||
Zampieri A</span><br />
|
||
<span class="medgenPMjournal">Prog Brain Res</span>
|
||
2015;221:191-212.
|
||
Epub 2015 Jun 30
|
||
doi: 10.1016/bs.pbr.2015.05.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26518079" target="_blank">26518079</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21575128">Mechanisms and treatment of primary angle closure: a review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ng WT,
|
||
Morgan W</span><br />
|
||
<span class="medgenPMjournal">Clin Exp Ophthalmol</span>
|
||
2012 May-Jun;40(4):e218-28.
|
||
Epub 2011 Jul 26
|
||
doi: 10.1111/j.1442-9071.2011.02604.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21575128" target="_blank">21575128</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/5647613">Shallow anterior chamber after cataract extraction. II. Treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pradhan JS,
|
||
Shukla BR,
|
||
Ahuja OP</span><br />
|
||
<span class="medgenPMjournal">Eye Ear Nose Throat Mon</span>
|
||
1968 Mar;47(3):139-43.
|
||
<span class="bold">PMID: </span><a href="/pubmed/5647613" target="_blank">5647613</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22shallow%20anterior%20chamber%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 (17)</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/38780279">Efficacy and Safety of Surgical Peripheral Iridectomy, Goniosynechialysis, and Goniotomy for Advanced Primary Angle Closure Glaucoma Without Cataract: 1-Year Results of a Multicenter Study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gao X,
|
||
Lin F,
|
||
Lu P,
|
||
Xie L,
|
||
Tang L,
|
||
Zhu X,
|
||
Zhang Y,
|
||
Lv A,
|
||
Tang G,
|
||
Zhang H,
|
||
Yan X,
|
||
Song Y,
|
||
Xu J,
|
||
Huang J,
|
||
Zhang Y,
|
||
Hu K,
|
||
Peng Y,
|
||
Wang Z,
|
||
Li X,
|
||
Chen W,
|
||
Wang N,
|
||
Barton K,
|
||
Park KH,
|
||
Aung T,
|
||
Weinreb RN,
|
||
Lam DSC,
|
||
Fan S,
|
||
Tham CC,
|
||
Zhang X;
|
||
TVG study group</span><br />
|
||
<span class="medgenPMjournal">J Glaucoma</span>
|
||
2024 Sep 1;33(9):632-639.
|
||
Epub 2024 May 24
|
||
doi: 10.1097/IJG.0000000000002443.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38780279" target="_blank">38780279</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38334238">Accuracy of 11 intraocular lens calculation formulas in shallow anterior chamber eyes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yuan H,
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Epub 2024 Feb 9
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doi: 10.1111/aos.16654.
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<span class="bold">PMID: </span><a href="/pubmed/38334238" target="_blank">38334238</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/36912740">Device-modified trabeculectomy for glaucoma.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Park J,
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Rittiphairoj T,
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Wang X,
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E JY,
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doi: 10.1002/14651858.CD010472.pub3.
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<span class="bold">PMID: </span><a href="/pubmed/36912740" target="_blank">36912740</a><a href="/pmc/articles/PMC10010250" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/35180153">Two-Year Outcomes of the Paul Glaucoma Implant for Treatment of Glaucoma.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Tan MCJ,
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Choy HYC,
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Koh Teck Chang V,
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Aquino MC,
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Sng CCA,
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Lim DKA,
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Loon SC,
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Chew Tec Kuan P</span><br />
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<span class="bold">PMID: </span><a href="/pubmed/35180153" target="_blank">35180153</a><a href="/pmc/articles/PMC9148669" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/29971817">Choroidal detachments: what do optometrists need to know?</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Diep MQ,
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Madigan MC</span><br />
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<span class="medgenPMjournal">Clin Exp Optom</span>
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<span class="bold">PMID: </span><a href="/pubmed/29971817" target="_blank">29971817</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Shallow%20anterior%20chamber%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 (275)</a></div><h3 class="subhead">Diagnosis</h3>
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<div class="nl"><a target="_blank" href="/pubmed/29971817">Choroidal detachments: what do optometrists need to know?</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Diep MQ,
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Madigan MC</span><br />
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<span class="medgenPMjournal">Clin Exp Optom</span>
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2019 Mar;102(2):116-125.
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Epub 2018 Jul 4
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doi: 10.1111/cxo.12807.
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<span class="bold">PMID: </span><a href="/pubmed/29971817" target="_blank">29971817</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/28772304">Acute-Onset Blurred Vision With Shallow Anterior Chamber and Suspected Choroidal Mass.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/36912740">Device-modified trabeculectomy for glaucoma.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Park J,
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Rittiphairoj T,
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E JY,
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Bicket AK</span><br />
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<span class="bold">PMID: </span><a href="/pubmed/36912740" target="_blank">36912740</a><a href="/pmc/articles/PMC10010250" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/29971817">Choroidal detachments: what do optometrists need to know?</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Diep MQ,
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Madigan MC</span><br />
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<span class="medgenPMjournal">Clin Exp Optom</span>
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2019 Mar;102(2):116-125.
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Epub 2018 Jul 4
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doi: 10.1111/cxo.12807.
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<span class="bold">PMID: </span><a href="/pubmed/29971817" target="_blank">29971817</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/28772304">Acute-Onset Blurred Vision With Shallow Anterior Chamber and Suspected Choroidal Mass.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Surakiatchanukul T,
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Roelofs KA,
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Shields CL</span><br />
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<div class="nl"><a target="_blank" href="/pubmed/24698625">Congenital uveal malignant melanoma.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/38334238">Accuracy of 11 intraocular lens calculation formulas in shallow anterior chamber eyes.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Yuan H,
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Zhang J,
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Han X,
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Ye J,
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Huang Y,
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Huang R,
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Wen L,
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Qiu X,
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Luo L</span><br />
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2024 Aug;102(5):e705-e711.
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Epub 2024 Feb 9
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doi: 10.1111/aos.16654.
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<span class="bold">PMID: </span><a href="/pubmed/38334238" target="_blank">38334238</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/37844256">Application of Femtosecond Laser in Challenging Cataract Cases.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Lee YW,
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Cho KS,
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Han SB</span><br />
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<span class="bold">PMID: </span><a href="/pubmed/37844256" target="_blank">37844256</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/35180153">Two-Year Outcomes of the Paul Glaucoma Implant for Treatment of Glaucoma.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Tan MCJ,
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Choy HYC,
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Koh Teck Chang V,
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Aquino MC,
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Sng CCA,
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Lim DKA,
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Loon SC,
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Chew Tec Kuan P</span><br />
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2022 Jun 1;31(6):449-455.
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Epub 2022 Feb 18
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doi: 10.1097/IJG.0000000000001998.
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<span class="bold">PMID: </span><a href="/pubmed/35180153" target="_blank">35180153</a><a href="/pmc/articles/PMC9148669" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
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<div class="nl"><a target="_blank" href="/pubmed/29971817">Choroidal detachments: what do optometrists need to know?</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Diep MQ,
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Madigan MC</span><br />
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<span class="medgenPMjournal">Clin Exp Optom</span>
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2019 Mar;102(2):116-125.
|
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Epub 2018 Jul 4
|
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doi: 10.1111/cxo.12807.
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<span class="bold">PMID: </span><a href="/pubmed/29971817" target="_blank">29971817</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/27801688">Current and effective advantages of femto phacoemulsification.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Agarwal A,
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Jacob S</span><br />
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doi: 10.1097/ICU.0000000000000333.
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<span class="bold">PMID: </span><a href="/pubmed/27801688" target="_blank">27801688</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Shallow%20anterior%20chamber%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 (130)</a></div><h3 class="subhead">Clinical prediction guides</h3>
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<div class="nl"><a target="_blank" href="/pubmed/38780279">Efficacy and Safety of Surgical Peripheral Iridectomy, Goniosynechialysis, and Goniotomy for Advanced Primary Angle Closure Glaucoma Without Cataract: 1-Year Results of a Multicenter Study.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Gao X,
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Lin F,
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Lu P,
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Xie L,
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Tang L,
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Zhu X,
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Zhang Y,
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Lv A,
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Tang G,
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Zhang H,
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Yan X,
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Song Y,
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Xu J,
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Huang J,
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Zhang Y,
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Hu K,
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Peng Y,
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Wang Z,
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Li X,
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Chen W,
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Wang N,
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Barton K,
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Park KH,
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Aung T,
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Weinreb RN,
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Lam DSC,
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Fan S,
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Tham CC,
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Zhang X;
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<span class="medgenPMjournal">J Glaucoma</span>
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2024 Sep 1;33(9):632-639.
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Epub 2024 May 24
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<span class="bold">PMID: </span><a href="/pubmed/38780279" target="_blank">38780279</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/38334238">Accuracy of 11 intraocular lens calculation formulas in shallow anterior chamber eyes.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Yuan H,
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Zhang J,
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Han X,
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Ye J,
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Huang Y,
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Huang R,
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Wen L,
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Qiu X,
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Chen X,
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Chen K,
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Tan X,
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Luo L</span><br />
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<span class="medgenPMjournal">Acta Ophthalmol</span>
|
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2024 Aug;102(5):e705-e711.
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Epub 2024 Feb 9
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doi: 10.1111/aos.16654.
|
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<span class="bold">PMID: </span><a href="/pubmed/38334238" target="_blank">38334238</a></div>
|
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|
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<div class="nl"><a target="_blank" href="/pubmed/37844256">Application of Femtosecond Laser in Challenging Cataract Cases.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Lee YW,
|
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Cho KS,
|
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Hyon JY,
|
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Han SB</span><br />
|
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<span class="medgenPMjournal">Asia Pac J Ophthalmol (Phila)</span>
|
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2023 Sep-Oct 01;12(5):477-485.
|
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Epub 2023 Aug 14
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doi: 10.1097/APO.0000000000000627.
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<span class="bold">PMID: </span><a href="/pubmed/37844256" target="_blank">37844256</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/33099746">Femtosecond laser-assisted cataract surgery in shallow anterior chamber cases.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Fernández-Vega Cueto A,
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Rodríguez-Una I,
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Alfonso JF</span><br />
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<span class="medgenPMjournal">Int Ophthalmol</span>
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<span class="bold">PMID: </span><a href="/pubmed/33099746" target="_blank">33099746</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/27801688">Current and effective advantages of femto phacoemulsification.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Agarwal A,
|
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Jacob S</span><br />
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<span class="medgenPMjournal">Curr Opin Ophthalmol</span>
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2017 Jan;28(1):49-57.
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doi: 10.1097/ICU.0000000000000333.
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<span class="bold">PMID: </span><a href="/pubmed/27801688" target="_blank">27801688</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Shallow%20anterior%20chamber%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 (112)</a></div></div>
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</div>
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<div class="portlet mgSection" id="ID_104">
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<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>
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<div class="portlet_content ln">
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<div class="nl"><a target="_blank" href="/pubmed/36912740">Device-modified trabeculectomy for glaucoma.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Park J,
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Rittiphairoj T,
|
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Wang X,
|
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E JY,
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Bicket AK</span><br />
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<span class="medgenPMjournal">Cochrane Database Syst Rev</span>
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2023 Mar 13;3(3):CD010472.
|
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doi: 10.1002/14651858.CD010472.pub3.
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<span class="bold">PMID: </span><a href="/pubmed/36912740" target="_blank">36912740</a><a href="/pmc/articles/PMC10010250" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/26769010">Anti-vascular endothelial growth factor for control of wound healing in glaucoma surgery.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Cheng JW,
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<div class="nl"><a target="_blank" href="/pubmed/25636153">Surgical interventions for primary congenital glaucoma.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Ghate D,
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|
||
<div class="nl"><a target="_blank" href="/pubmed/24158640">Efficacy and safety of trabeculectomy vs nonpenetrating surgical procedures: a systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rulli E,
|
||
Biagioli E,
|
||
Riva I,
|
||
Gambirasio G,
|
||
De Simone I,
|
||
Floriani I,
|
||
Quaranta L</span><br />
|
||
<span class="medgenPMjournal">JAMA Ophthalmol</span>
|
||
2013 Dec;131(12):1573-82.
|
||
doi: 10.1001/jamaophthalmol.2013.5059.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24158640" target="_blank">24158640</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22029538">Intraoperative mitomycin C versus intraoperative 5-fluorouracil for trabeculectomy: a systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lin ZJ,
|
||
Li Y,
|
||
Cheng JW,
|
||
Lu XH</span><br />
|
||
<span class="medgenPMjournal">J Ocul Pharmacol Ther</span>
|
||
2012 Apr;28(2):166-73.
|
||
Epub 2011 Oct 26
|
||
doi: 10.1089/jop.2011.0117.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22029538" target="_blank">22029538</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Shallow%20anterior%20chamber%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 (7)</a></div></div>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C0423276%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (4)</a></li>
|
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<li><a href="/gtr/tests?term=C0423276%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (4)</a></li>
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<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C0423276%5bDISCUI%5d" target="_blank">See all (4)</a></total></li>
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