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<meta name="keywords" content="C1842914, adult onset vitelliform dystrophy, adult onset vitelliform macular dystrophy, adult vitelliform macular dystrophy, adult-onset foveomacular dystrophies, adult-onset foveomacular dystrophy, adult-onset foveomacular dystrophy with choroidal neovascularization, adult-onset foveomacular vitelliform dystrophy, adult-onset vitelliform macular dystrophy, aofmd, aofmd - adult-onset foveomacular dystrophy, avmd, avmd - adult vitelliform macular dystrophy, disease or syndrome, dystrophies, adult-onset foveomacular, dystrophy, adult-onset foveomacular, foveomacular dystrophies, adult-onset, foveomacular dystrophy, adult onset, foveomacular dystrophy, adult-onset, foveomacular dystrophy, adult-onset, with choroidal neovascularization, foveomacular dystrophy, adult-onset, with or without choroidal neovascularization, foveomacular dystrophy, adult-onset; aofmd, gass disease, macular dystrophy, vitelliform, 3, macular dystrophy, vitelliform, adult-onset, macular dystrophy, vitelliform, type 3, pseudo-best disease, pseudo-vitelliform macular dystrophy, vitelliform macular dystrophy, adult onset, vitelliform macular dystrophy, adult-onset, vmd3, 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="Adult-onset foveomacular vitelliform dystrophy, also known as adult vitelliform macular dystrophy, adult-type foveomacular dystrophy, adult vitelliform macular degeneration, pseudovitelliform macular degeneration, and adult-onset foveomacular pigment epithelial dystrophy, is characterized by a solitary, oval, slightly elevated yellowish subretinal lesion of the fovea that is similar in appearance to the vitelliform or egg-yolk stage of Best disease (153700). Initially the yellow lesion may be present in only one eye. The size is generally one-third to one disc diameter, and small yellow flecks are seen in the paracentral lesion. Patients usually become symptomatic in the fourth or fifth decade of life with a protracted decrease of visual acuity and mild metamorphopsia. Electrooculographic testing reveals a normal or only slightly reduced Arden ratio, which is intensely abnormal in Best disease. The prognosis is optimistic, as most patients retain reading vision throughout life (Felbor et al., 1997; Yamaguchi et al., 2001). For a discussion of genetic heterogeneity of vitelliform macular dystrophy, see VMD1 (153840)." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=334280
|
||
ConceptID=C1842914
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Adult-onset foveomacular vitelliform dystrophy<span class="h1sub">(AOFMD; VMD3; AVMD)</span></div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>334280</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:">C1842914</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Adult onset vitelliform dystrophy; FOVEOMACULAR DYSTROPHY, ADULT-ONSET; FOVEOMACULAR DYSTROPHY, ADULT-ONSET, WITH OR WITHOUT CHOROIDAL NEOVASCULARIZATION; Macular dystrophy, vitelliform, adult-onset</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Adult vitelliform macular dystrophy (232049001); Adult-onset foveomacular dystrophy (232049001); AOFMD - adult-onset foveomacular dystrophy (232049001); AVMD - adult vitelliform macular dystrophy (232049001); Gass disease (232049001); Pseudo-Best disease (232049001); Pseudo-vitelliform macular dystrophy (232049001); Adult-onset vitelliform macular dystrophy (232049001)</td></tr>
|
||
<tr><td>Modes of inheritance:</td>
|
||
<td>
|
||
<div class="divPopper rprt" id="moi_141047"><div><strong>Autosomal dominant inheritance</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>141047</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.">C0443147</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Intellectual Product</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Source: Orphanet</div>
|
||
<div class="spaceAbove">A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.</div></div>
|
||
<div class="divPopper rprt" id="moi_988794"><div><strong>Not genetically inherited</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>988794</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier assigned by MedGen (starting with CN) for terms that cannot be identified in NLM's Unified Medical Language system (UMLS) Click for more information.">CN307044</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Source: Orphanet</div>
|
||
<div class="spaceAbove">clinical entity without genetic inheritance.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/988794">This record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#moi_141047" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal dominant inheritance</a><span> (Orphanet)</span></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#moi_988794" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Not genetically inherited</a><span> (Orphanet)</span></div></td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td><a class="help" data-jig="ncbipopper" href="#target-gene-related">Related genes:<img src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a><div id="target-gene-related" class="display-none">
|
||
Gene(s) associated with related conditions. For conditions<br />
|
||
in a hierarchy, the parent condition will list the genes<br />
|
||
associated with the children conditions.</div></td>
|
||
<td><a target="_blank" href="/gene/50939">IMPG2</a>, <a target="_blank" href="/gene/5961">PRPH2</a>, <a target="_blank" href="/gene/3617">IMPG1</a></td></tr><tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0011979" target="_blank">MONDO:0011979</a></td></tr>
|
||
<tr><td>OMIM<span class="superscript">®</span>:</td>
|
||
<td><a href="https://omim.org/entry/179605" target="_blank">179605</a>; <a href="https://omim.org/entry/608161" target="_blank">608161</a></td></tr>
|
||
<tr><td>Orphanet:</td>
|
||
<td><a target="_blank" title="Orphanet: The portal for rare diseases and orphan drugs" href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=99000">ORPHA99000</a></td></tr></tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
|
||
<div class="portlet mgSection" id="ID_100">
|
||
<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">Adult-onset foveomacular vitelliform dystrophy, also known as adult vitelliform macular dystrophy, adult-type foveomacular dystrophy, adult vitelliform macular degeneration, pseudovitelliform macular degeneration, and adult-onset foveomacular pigment epithelial dystrophy, is characterized by a solitary, oval, slightly elevated yellowish subretinal lesion of the fovea that is similar in appearance to the vitelliform or egg-yolk stage of Best disease (153700). Initially the yellow lesion may be present in only one eye. The size is generally one-third to one disc diameter, and small yellow flecks are seen in the paracentral lesion. Patients usually become symptomatic in the fourth or fifth decade of life with a protracted decrease of visual acuity and mild metamorphopsia. Electrooculographic testing reveals a normal or only slightly reduced Arden ratio, which is intensely abnormal in Best disease. The prognosis is optimistic, as most patients retain reading vision throughout life (Felbor et al., 1997; Yamaguchi et al., 2001). For a discussion of genetic heterogeneity of vitelliform macular dystrophy, see VMD1 (153840). [from <a title="Online Mendelian Inheritance in Man" href="http://www.omim.org" class="defSource" target="_blank">OMIM</a>]</div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_117">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Additional_description">Additional description</h1><a sid="117" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><div class="mgSection"><strong>From MedlinePlus Genetics</strong><br />Researchers have described two forms of vitelliform macular dystrophy with similar features. The early-onset form (known as Best disease) usually appears in childhood; the age at which symptoms begin and the severity of vision loss vary widely. The adult-onset form begins later, usually in mid-adulthood, and tends to cause vision loss that worsens slowly over time. The two forms of vitelliform macular dystrophy each have characteristic changes in the macula that can be detected during an eye examination.<br /><br />Vitelliform macular dystrophy causes a fatty yellow pigment (called lipofuscin) to build up in cells underlying the macula. Over time, large amounts of this substance can damage cells that are critical for clear central vision. As a result, people with this disorder often lose their central vision, and their eyesight may become blurry or distorted. Vitelliform macular dystrophy typically does not affect side (peripheral) vision or the ability to see at night.<br /><br />Vitelliform macular dystrophy is a genetic eye disorder that can cause worsening (progressive) vision loss. This disorder affects the retina, the specialized light-sensitive tissue that lines the back of the eye. Specifically, vitelliform macular dystrophy disrupts cells in a small area near the center of the retina called the macula. The macula is responsible for sharp central vision, which is needed for detailed tasks such as reading, driving, and recognizing faces. <a target="_blank" href="https://medlineplus.gov/genetics/condition/vitelliform-macular-dystrophy">https://medlineplus.gov/genetics/condition/vitelliform-macular-dystrophy</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_102">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_features">Clinical features</h1><a sid="102" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat"><strong>From HPO</strong><br />
|
||
<div class="divPopper rprt" id="clin_43220"><div><strong>Photophobia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>43220</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.">C0085636</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Sign or Symptom</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Excessive sensitivity to light with the sensation of discomfort or pain in the eyes due to exposure to bright light.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/43220">Feature record</a> | <a href="/medgen?term=%22Photophobia%22%5BClinical%20Features%5D%20OR%2043220%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_115964"><div><strong>Color vision defect</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>115964</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.">C0234629</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">An anomaly in the ability to discriminate between or recognize colors.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/115964">Feature record</a> | <a href="/medgen?term=%22Color%20vision%20defect%22%5BClinical%20Features%5D%20OR%20115964%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_65889"><div><strong>Reduced visual acuity</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>65889</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.">C0234632</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Diminished clarity of vision.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/65889">Feature record</a> | <a href="/medgen?term=%22Reduced%20visual%20acuity%22%5BClinical%20Features%5D%20OR%2065889%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_75739"><div><strong>Metamorphopsia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75739</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.">C0271185</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Sign or Symptom</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A visual anomaly in which images appear distorted. A grid of straight lines appears wavy and parts of the grid may appear blank.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/75739">Feature record</a> | <a href="/medgen?term=%22Metamorphopsia%22%5BClinical%20Features%5D%20OR%2075739%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_140841"><div><strong>Macular atrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>140841</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.">C0423421</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Well-demarcated area(s) of partial or complete depigmentation in the macula, reflecting atrophy of the retinal pigment epithelium with associated retinal photoreceptor loss.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/140841">Feature record</a> | <a href="/medgen?term=%22Macular%20atrophy%22%5BClinical%20Features%5D%20OR%20140841%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_154726"><div><strong>Choroidal neovascularization</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>154726</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.">C0600518</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Pathologic Function</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Choroidal neovascularization (CNV) is the creation of new blood vessels in the choroid layer of the eye.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/154726">Feature record</a> | <a href="/medgen?term=%22Choroidal%20neovascularization%22%5BClinical%20Features%5D%20OR%20154726%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_196451"><div><strong>Macular dystrophy</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>196451</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.">C0730292</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Macular dystrophy is a nonspecific term for premature retinal cell aging and cell death, generally confied to the macula in which no clear extrinsic cause is evident.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/196451">Feature record</a> | <a href="/medgen?term=%22Macular%20dystrophy%22%5BClinical%20Features%5D%20OR%20196451%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_488956"><div><strong>Drusen</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>488956</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.">C1260959</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Drusen (singular, 'druse') are tiny yellow or white accumulations of extracellular material (lipofuscin) that build up in Bruch's membrane of the eye.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/488956">Feature record</a> | <a href="/medgen?term=%22Drusen%22%5BClinical%20Features%5D%20OR%20488956%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_777085"><div><strong>Visual impairment</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>777085</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.">C3665347</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Visual impairment (or vision impairment) is vision loss (of a person) to such a degree as to qualify as an additional support need through a significant limitation of visual capability resulting from either disease, trauma, or congenital or degenerative conditions that cannot be corrected by conventional means, such as refractive correction, medication, or surgery.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/777085">Feature record</a> | <a href="/medgen?term=%22Visual%20impairment%22%5BClinical%20Features%5D%20OR%20777085%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_892486"><div><strong>Vitelliform-like macular lesions</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>892486</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.">C4024817</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Vitelliform maculopathy is a sharply demarcated lesion caused by the accumulation of material, often lipofuscin in the subretinal space underlying the macula.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/892486">Feature record</a> | <a href="/medgen?term=%22Vitelliform-like%20macular%20lesions%22%5BClinical%20Features%5D%20OR%20892486%5Buid%5D">Search on this feature</a></div></div><div class="TreeLite" data-jigconfig="closed: 1"><div class="concept-def"><a class="small" href="#" onclick="jQuery(".TreeLite","#ID_102").TreeLite().openAll(); return false;">Show all</a><a class="small" href="#" onclick="jQuery(".TreeLite","#ID_102").TreeLite().closeAll(); return false;">Hide all</a></div><ul><li><span class="TLline">Abnormality of the eye</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_154726" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Choroidal neovascularization</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_115964" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Color vision defect</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_488956" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Drusen</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_140841" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Macular atrophy</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_196451" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Macular dystrophy</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_75739" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Metamorphopsia</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_65889" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Reduced visual acuity</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_777085" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Visual impairment</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_892486" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Vitelliform-like macular lesions</a></span></li></ul></li><li><span class="TLline">Abnormality of the nervous system</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_43220" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Photophobia</a></span></li></ul></li></ul></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_118">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li><li><a href="#tabORDO">Orphanet</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0339510[DISCUI]&test_type=Clinical" ref="ncbi_uid=137920">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 Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=137920" ref="ncbi_uid=137920">V</a></span></span><span class="TLline"><a href="/medgen/137920" ref="tree=GTR&ncbi_uid=137920&link_uid=137920" title="View MedGen record for 'Vitelliform macular dystrophy'">Vitelliform macular dystrophy</a></span><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C1842914[DISCUI]&test_type=Clinical" ref="ncbi_uid=334280">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=334280" target="_blank" href="/omim/179605">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=334280" ref="ncbi_uid=334280">V</a></span></span><span class="TLline">Adult-onset foveomacular vitelliform dystrophy</span><ul><li class="TLclosed"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=1636950" target="_blank" href="/omim/153840">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=1636950" ref="ncbi_uid=1636950">V</a></span></span><span class="TLline"><a href="/medgen/1636950" ref="tree=GTR&ncbi_uid=1636950&link_uid=1636950" title="View MedGen record for 'Vitelliform macular dystrophy 1'">Vitelliform macular dystrophy 1</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=CN295869[DISCUI]&test_type=Clinical" ref="ncbi_uid=979022">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 Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=979022" ref="ncbi_uid=979022">V</a></span></span><span class="TLline"><a href="/medgen/979022" ref="tree=GTR&ncbi_uid=979022&link_uid=979022" title="View MedGen record for 'Vitelliform macular dystrophy 3'">Vitelliform macular dystrophy 3</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C4015342[DISCUI]&test_type=Clinical" ref="ncbi_uid=863779">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=863779" target="_blank" href="/omim/602870">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=863779" ref="ncbi_uid=863779">V</a></span></span><span class="TLline"><a href="/medgen/863779" ref="tree=GTR&ncbi_uid=863779&link_uid=863779" title="View MedGen record for 'Vitelliform macular dystrophy 4'">Vitelliform macular dystrophy 4</a></span></li><li class="TLclosed"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C4015343[DISCUI]&test_type=Clinical" ref="ncbi_uid=863780">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet Ocolor" title="OMIM"><a ref="ncbi_uid=863780" target="_blank" href="/omim/607056">O</a></span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=863780" ref="ncbi_uid=863780">V</a></span></span><span class="TLline"><a href="/medgen/863780" ref="tree=GTR&ncbi_uid=863780&link_uid=863780" title="View MedGen record for 'Vitelliform macular dystrophy 5'">Vitelliform macular dystrophy 5</a></span></li></ul></li></ul></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/357005" ref="tree=MeSH" title="MedGen record for Patterned dystrophy of the retinal pigment epithelium">Patterned dystrophy of the retinal pigment epithelium</a></span><ul><li><span class="matched_ds">Adult-onset foveomacular vitelliform dystrophy</span><ul><li><span class="TLline"><a href="/medgen/1636950" ref="tree=MeSH" title="MedGen record for Vitelliform macular dystrophy 1">Vitelliform macular dystrophy 1</a></span></li><li><span class="TLline"><a href="/medgen/979022" ref="tree=MeSH" title="MedGen record for Vitelliform macular dystrophy 3">Vitelliform macular dystrophy 3</a></span></li><li><span class="TLline"><a href="/medgen/863779" ref="tree=MeSH" title="MedGen record for Vitelliform macular dystrophy 4">Vitelliform macular dystrophy 4</a></span></li><li><span class="TLline"><a href="/medgen/863780" ref="tree=MeSH" title="MedGen record for Vitelliform macular dystrophy 5">Vitelliform macular dystrophy 5</a></span></li></ul></li></ul></li></ul></div></div><div id="tabORDO">Follow <a target="_blank" href="http://www.orpha.net/consor/cgi-bin/Disease_Classif.php?lng=EN&data_id=156&PatId=14017&search=Disease_Classif_Simple&new=1" class="ital bold">this link</a> to review classifications for <span class="ital">Adult-onset foveomacular vitelliform dystrophy</span> in Orphanet.</div></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/24846624">Bevacizumab treatment for choroidal neovascularization associated with adult-onset foveomacular vitelliform dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tiosano L,
|
||
Jaouni T,
|
||
Averbukh E,
|
||
Grunin M,
|
||
Banin E,
|
||
Chowers I</span><br />
|
||
<span class="medgenPMjournal">Eur J Ophthalmol</span>
|
||
2014 Nov-Dec;24(6):890-6.
|
||
Epub 2014 May 20
|
||
doi: 10.5301/ejo.5000486.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24846624" target="_blank">24846624</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22adult-onset%20foveomacular%20vitelliform%20dystrophy%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 (1)</a></div><h3 class="subhead">Curated<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpCurated"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/22234150">Clinical utility gene card for: BEST1-related dystrophies (Bestrophinopathies).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ramsden SC,
|
||
Davidson AE,
|
||
Leroy BP,
|
||
Moore AT,
|
||
Webster AR,
|
||
Black GC,
|
||
Manson FD</span><br />
|
||
<span class="medgenPMjournal">Eur J Hum Genet</span>
|
||
2012 May;20(5)
|
||
Epub 2012 Jan 11
|
||
doi: 10.1038/ejhg.2011.251.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22234150" target="_blank">22234150</a><a href="/pmc/articles/PMC3330226" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=" title="PubMed search"></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/39585675">Adult Onset Foveomacular Vitelliform Dystrophy Shows Genetic Overlap With Age-Related Macular Degeneration.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jaskoll S,
|
||
Kramer A,
|
||
Elbaz-Hayoun S,
|
||
Rinsky B,
|
||
Eandi CM,
|
||
Grunin M,
|
||
Shwartz Y,
|
||
Tiosano L,
|
||
Heid IM,
|
||
Winkler T,
|
||
Chowers I</span><br />
|
||
<span class="medgenPMjournal">Invest Ophthalmol Vis Sci</span>
|
||
2024 Nov 4;65(13):53.
|
||
doi: 10.1167/iovs.65.13.53.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39585675" target="_blank">39585675</a><a href="/pmc/articles/PMC11601137" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38066097">Retinal sensitivity and fundus autofluorescence in adult-onset foveomacular vitelliform dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fujino R,
|
||
Inoue T,
|
||
Yanagi Y,
|
||
Maruyama-Inoue M,
|
||
Kadonosono K,
|
||
Obata R,
|
||
Asaoka R</span><br />
|
||
<span class="medgenPMjournal">Sci Rep</span>
|
||
2023 Dec 8;13(1):21777.
|
||
doi: 10.1038/s41598-023-49256-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38066097" target="_blank">38066097</a><a href="/pmc/articles/PMC10709410" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37067692">The pseudohypopyon stage in adult-onset foveomacular vitelliform dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shmueli O,
|
||
Lender R,
|
||
Shwartz Y,
|
||
Chowers I,
|
||
Tiosano L</span><br />
|
||
<span class="medgenPMjournal">Int Ophthalmol</span>
|
||
2023 Sep;43(9):3107-3113.
|
||
Epub 2023 Apr 17
|
||
doi: 10.1007/s10792-023-02710-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37067692" target="_blank">37067692</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30578490">Pattern Dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tsang SH,
|
||
Sharma T</span><br />
|
||
<span class="medgenPMjournal">Adv Exp Med Biol</span>
|
||
2018;1085:91-96.
|
||
doi: 10.1007/978-3-319-95046-4_17.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30578490" target="_blank">30578490</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28198786">OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY IN ADULT-ONSET FOVEOMACULAR VITELLIFORM DYSTROPHY.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Joshi KM,
|
||
Nesper PL,
|
||
Fawzi AA,
|
||
Mirza RG</span><br />
|
||
<span class="medgenPMjournal">Retina</span>
|
||
2018 Mar;38(3):600-605.
|
||
doi: 10.1097/IAE.0000000000001565.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28198786" target="_blank">28198786</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Adult-onset%20foveomacular%20vitelliform%20dystrophy%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 (47)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38066097">Retinal sensitivity and fundus autofluorescence in adult-onset foveomacular vitelliform dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fujino R,
|
||
Inoue T,
|
||
Yanagi Y,
|
||
Maruyama-Inoue M,
|
||
Kadonosono K,
|
||
Obata R,
|
||
Asaoka R</span><br />
|
||
<span class="medgenPMjournal">Sci Rep</span>
|
||
2023 Dec 8;13(1):21777.
|
||
doi: 10.1038/s41598-023-49256-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38066097" target="_blank">38066097</a><a href="/pmc/articles/PMC10709410" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37067692">The pseudohypopyon stage in adult-onset foveomacular vitelliform dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shmueli O,
|
||
Lender R,
|
||
Shwartz Y,
|
||
Chowers I,
|
||
Tiosano L</span><br />
|
||
<span class="medgenPMjournal">Int Ophthalmol</span>
|
||
2023 Sep;43(9):3107-3113.
|
||
Epub 2023 Apr 17
|
||
doi: 10.1007/s10792-023-02710-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37067692" target="_blank">37067692</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28198786">OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY IN ADULT-ONSET FOVEOMACULAR VITELLIFORM DYSTROPHY.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Joshi KM,
|
||
Nesper PL,
|
||
Fawzi AA,
|
||
Mirza RG</span><br />
|
||
<span class="medgenPMjournal">Retina</span>
|
||
2018 Mar;38(3):600-605.
|
||
doi: 10.1097/IAE.0000000000001565.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28198786" target="_blank">28198786</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25681578">Adult-onset foveomacular vitelliform dystrophy: A fresh perspective.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chowers I,
|
||
Tiosano L,
|
||
Audo I,
|
||
Grunin M,
|
||
Boon CJ</span><br />
|
||
<span class="medgenPMjournal">Prog Retin Eye Res</span>
|
||
2015 Jul;47:64-85.
|
||
Epub 2015 Feb 11
|
||
doi: 10.1016/j.preteyeres.2015.02.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25681578" target="_blank">25681578</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15097895">Deposition of yellow submacular material in central serous chorioretinopathy resembling adult-onset foveomacular vitelliform dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Spaide RF</span><br />
|
||
<span class="medgenPMjournal">Retina</span>
|
||
2004 Apr;24(2):301-4.
|
||
doi: 10.1097/00006982-200404000-00019.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15097895" target="_blank">15097895</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Adult-onset%20foveomacular%20vitelliform%20dystrophy%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 (55)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34240658">Clinical and molecular findings in patients with pattern dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sodi A,
|
||
Mucciolo DP,
|
||
Giorgio D,
|
||
Passerini I,
|
||
Pacini B,
|
||
Bruschi M,
|
||
Verdina T,
|
||
Virgili G,
|
||
Giansanti F,
|
||
Murro V</span><br />
|
||
<span class="medgenPMjournal">Ophthalmic Genet</span>
|
||
2021 Oct;42(5):577-587.
|
||
Epub 2021 Jul 9
|
||
doi: 10.1080/13816810.2021.1938140.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34240658" target="_blank">34240658</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29195727">Clinical and imaging findings of pattern dystrophy subtypes; Diagnostic errors and unnecessary treatment in clinical practice.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ozkaya A,
|
||
Garip R,
|
||
Nur Tarakcioglu H,
|
||
Alkin Z,
|
||
Taskapili M</span><br />
|
||
<span class="medgenPMjournal">J Fr Ophtalmol</span>
|
||
2018 Jan;41(1):21-29.
|
||
Epub 2017 Nov 28
|
||
doi: 10.1016/j.jfo.2017.06.009.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29195727" target="_blank">29195727</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24846624">Bevacizumab treatment for choroidal neovascularization associated with adult-onset foveomacular vitelliform dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tiosano L,
|
||
Jaouni T,
|
||
Averbukh E,
|
||
Grunin M,
|
||
Banin E,
|
||
Chowers I</span><br />
|
||
<span class="medgenPMjournal">Eur J Ophthalmol</span>
|
||
2014 Nov-Dec;24(6):890-6.
|
||
Epub 2014 May 20
|
||
doi: 10.5301/ejo.5000486.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24846624" target="_blank">24846624</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23400081">Ranibizumab for choroidal neovascularization associated with adult-onset foveomacular vitelliform dystrophy: one-year results.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mimoun G,
|
||
Caillaux V,
|
||
Querques G,
|
||
Rothschild PR,
|
||
Puche N,
|
||
Souied EH</span><br />
|
||
<span class="medgenPMjournal">Retina</span>
|
||
2013 Mar;33(3):513-21.
|
||
doi: 10.1097/IAE.0b013e3182753adb.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23400081" target="_blank">23400081</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20931215">Primary intravitreal ranibizumab for adult-onset foveomacular vitelliform dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gallego-Pinazo R,
|
||
Dolz-Marco R,
|
||
Pardo-López D,
|
||
Arevalo JF,
|
||
Díaz-Llopis M</span><br />
|
||
<span class="medgenPMjournal">Graefes Arch Clin Exp Ophthalmol</span>
|
||
2011 Mar;249(3):455-8.
|
||
Epub 2010 Oct 8
|
||
doi: 10.1007/s00417-010-1536-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20931215" target="_blank">20931215</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Adult-onset%20foveomacular%20vitelliform%20dystrophy%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 (10)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/28198786">OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY IN ADULT-ONSET FOVEOMACULAR VITELLIFORM DYSTROPHY.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Joshi KM,
|
||
Nesper PL,
|
||
Fawzi AA,
|
||
Mirza RG</span><br />
|
||
<span class="medgenPMjournal">Retina</span>
|
||
2018 Mar;38(3):600-605.
|
||
doi: 10.1097/IAE.0000000000001565.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28198786" target="_blank">28198786</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26951771">Optical coherence tomography angiography in adult-onset foveomacular vitelliform dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Querques G,
|
||
Zambrowski O,
|
||
Corvi F,
|
||
Miere A,
|
||
Semoun O,
|
||
Srour M,
|
||
Souied EH</span><br />
|
||
<span class="medgenPMjournal">Br J Ophthalmol</span>
|
||
2016 Dec;100(12):1724-1730.
|
||
Epub 2016 Mar 7
|
||
doi: 10.1136/bjophthalmol-2016-308370.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26951771" target="_blank">26951771</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23400081">Ranibizumab for choroidal neovascularization associated with adult-onset foveomacular vitelliform dystrophy: one-year results.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mimoun G,
|
||
Caillaux V,
|
||
Querques G,
|
||
Rothschild PR,
|
||
Puche N,
|
||
Souied EH</span><br />
|
||
<span class="medgenPMjournal">Retina</span>
|
||
2013 Mar;33(3):513-21.
|
||
doi: 10.1097/IAE.0b013e3182753adb.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23400081" target="_blank">23400081</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21664595">Natural course of adult-onset foveomacular vitelliform dystrophy: a spectral-domain optical coherence tomography analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Querques G,
|
||
Forte R,
|
||
Querques L,
|
||
Massamba N,
|
||
Souied EH</span><br />
|
||
<span class="medgenPMjournal">Am J Ophthalmol</span>
|
||
2011 Aug;152(2):304-13.
|
||
Epub 2011 Jun 12
|
||
doi: 10.1016/j.ajo.2011.01.047.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21664595" target="_blank">21664595</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16567277">Adult-onset foveomacular vitelliform dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Do P,
|
||
Ferrucci S</span><br />
|
||
<span class="medgenPMjournal">Optometry</span>
|
||
2006 Apr;77(4):156-66.
|
||
doi: 10.1016/j.optm.2006.01.020.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16567277" target="_blank">16567277</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Adult-onset%20foveomacular%20vitelliform%20dystrophy%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 (19)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39585675">Adult Onset Foveomacular Vitelliform Dystrophy Shows Genetic Overlap With Age-Related Macular Degeneration.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jaskoll S,
|
||
Kramer A,
|
||
Elbaz-Hayoun S,
|
||
Rinsky B,
|
||
Eandi CM,
|
||
Grunin M,
|
||
Shwartz Y,
|
||
Tiosano L,
|
||
Heid IM,
|
||
Winkler T,
|
||
Chowers I</span><br />
|
||
<span class="medgenPMjournal">Invest Ophthalmol Vis Sci</span>
|
||
2024 Nov 4;65(13):53.
|
||
doi: 10.1167/iovs.65.13.53.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39585675" target="_blank">39585675</a><a href="/pmc/articles/PMC11601137" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38461930">Risk Factors for Worsening Morphology and Visual Acuity in Eyes with Adult-Onset Foveomacular Vitelliform Dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nipp GE,
|
||
Sarici K,
|
||
Lee T,
|
||
Hadziahmetovic M</span><br />
|
||
<span class="medgenPMjournal">Ophthalmol Retina</span>
|
||
2024 Aug;8(8):804-812.
|
||
Epub 2024 Mar 8
|
||
doi: 10.1016/j.oret.2024.03.004.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38461930" target="_blank">38461930</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28573994">Microperimetric evaluation in patients with adult-onset foveomacular vitelliform dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Grenga PL,
|
||
Fragiotta S,
|
||
Cutini A,
|
||
Meduri A,
|
||
Vingolo EM</span><br />
|
||
<span class="medgenPMjournal">Indian J Ophthalmol</span>
|
||
2017 May;65(5):385-389.
|
||
doi: 10.4103/ijo.IJO_984_16.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28573994" target="_blank">28573994</a><a href="/pmc/articles/PMC5565886" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27640006">Clinical Characteristics, Choroidal Neovascularization, and Predictors of Visual Outcomes in Acquired Vitelliform Lesions.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Balaratnasingam C,
|
||
Hoang QV,
|
||
Inoue M,
|
||
Curcio CA,
|
||
Dolz-Marco R,
|
||
Yannuzzi NA,
|
||
Dhrami-Gavazi E,
|
||
Yannuzzi LA,
|
||
Freund KB</span><br />
|
||
<span class="medgenPMjournal">Am J Ophthalmol</span>
|
||
2016 Dec;172:28-38.
|
||
Epub 2016 Sep 14
|
||
doi: 10.1016/j.ajo.2016.09.008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27640006" target="_blank">27640006</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26951771">Optical coherence tomography angiography in adult-onset foveomacular vitelliform dystrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Querques G,
|
||
Zambrowski O,
|
||
Corvi F,
|
||
Miere A,
|
||
Semoun O,
|
||
Srour M,
|
||
Souied EH</span><br />
|
||
<span class="medgenPMjournal">Br J Ophthalmol</span>
|
||
2016 Dec;100(12):1724-1730.
|
||
Epub 2016 Mar 7
|
||
doi: 10.1136/bjophthalmol-2016-308370.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26951771" target="_blank">26951771</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Adult-onset%20foveomacular%20vitelliform%20dystrophy%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 (32)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
</div>
|
||
<div class=" bottom">
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||
|
||
</div>
|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
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|
||
|
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<div class="rightCol mgCol">
|
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<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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|
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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=C1842914%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (22)</a></li>
|
||
<li><a href="/gtr/tests?term=C1842914%5bDISCUI%5d&filter=method%3A2%5F17" target="_blank">Mutation scanning of the entire coding region (1)</a></li>
|
||
<li><a href="/gtr/tests?term=C1842914%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (30)</a></li>
|
||
<li><a href="/gtr/tests?term=C1842914%5bDISCUI%5d&filter=method%3A2%5F19" target="_blank">Targeted variant analysis (6)</a></li>
|
||
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C1842914%5bDISCUI%5d" target="_blank">See all (37)</a></total></li>
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<div class="portlet_content ln"><ul><li><a href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=99000" target="_blank">Orphanet</a></li><li><a href="https://clinicaltrials.gov/search?cond=Adult-onset%20foveomacular%20vitelliform%20dystrophy" target="_blank">ClinicalTrials.gov</a></li></ul></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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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22adult-onset%20foveomacular%20vitelliform%20dystrophy%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Adult-onset%20foveomacular%20vitelliform%20dystrophy%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul><h3 class="subhead">Curated</h3><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov//22234150/">EuroGentest, 2012</a><div>Clinical utility gene card for: BEST1-related dystrophies (Bestrophinopathies).</div></li></ul></div>
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||
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|
||
<div class="portlet_content ln"><ul><li><a href="http://www.diseaseinfosearch.org/Adult-onset+vitelliform+macular+dystrophy/8779" target="_blank">Genetic Alliance</a></li><li><a href="https://www.malacards.org/card/macular_dystrophy_vitelliform_3" target="_blank">MalaCards</a></li><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Adult-onset%20foveomacular%20vitelliform%20dystrophy" target="_blank">MedlinePlus</a></li><li><a href="https://medlineplus.gov/genetics/condition/vitelliform-macular-dystrophy" target="_blank">MedlinePlusGenetics (GHR)</a></li><li><a href="https://rarediseases.info.nih.gov/diseases/10909/disease" target="_blank">NCATS Office of Rare Diseases Research (GARD)</a></li></ul></div>
|
||
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|
||
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|
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|
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<a href="/pubmed/clinical?term=Adult-onset%20foveomacular%20vitelliform%20dystrophy" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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<a href="/pubmed?term=Adult-onset%20foveomacular%20vitelliform%20dystrophy%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=2" target="_blank">Reviews in PubMed</a>
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|
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<h3>Related information</h3>
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|
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<a class="brieflinkpopperctrl" href="/clinvar?LinkName=medgen_clinvar&from_uid=334280" ref="log$=recordlinks">ClinVar</a>
|
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<div class="brieflinkpop offscreen_noflow">Related medical variations</div>
|
||
</li>
|
||
<li class="brieflinkpopper">
|
||
<a class="brieflinkpopperctrl" href="/gtr/tests?term=C1842914[DISCUI]" ref="log$=recordlinks">GTR</a>
|
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<div class="brieflinkpop offscreen_noflow">Related information in GTR</div>
|
||
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|
||
<li class="brieflinkpopper">
|
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<a class="brieflinkpopperctrl" href="/gtr/tests?term=C1842914[DISCUI]&test_type=Clinical" ref="log$=recordlinks">GTR(Clinical)</a>
|
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|
||
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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed_omim&from_uid=334280" ref="log$=recordlinks">PubMed (OMIM)</a>
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||
<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67cb4668b15b832ebcc736c5">Adult-onset foveomacular vitelliform dystrophy</a>
|
||
<div class="ralinkpop offscreen_noflow">Adult-onset foveomacular vitelliform dystrophy<div class="brieflinkpopdesc"></div></div>
|
||
<div class="tertiary">MedGen</div>
|
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|
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|
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<a class="htb" ref="log$=activity&linkpos=2" href="/portal/utils/pageresolver.fcgi?recordid=67cb4667b15b832ebcc731a8">C1842914[conceptid] <span class="number">(1)</span></a>
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=3" href="/portal/utils/pageresolver.fcgi?recordid=67cb4666b15b832ebcc72c55">C1868512[trait identifier] AND "Illumina Laboratory Services, Ill... <span class="number">(43)</span></a>
|
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