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<!--
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UID=83290
|
||
ConceptID=C0339555
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Congenital hypertrophy of retinal pigment epithelium</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>83290</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.">C0339555</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality; Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Congenital hypertrophy of retinal pigment epithelium (CHRPE)</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>CHRPE - Congenital hypertrophy of retinal pigment epithelium (232074003); Congenital hyperplasia of retinal pigment epithelium (232074003); Congenital hypertrophy of retinal pigment epithelium (232074003)</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:0007649">HP:0007649</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>
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<div class="portlet_content ln">Sharply demarcated, congenital hyperpigmentation of the retinal pigment epithelium. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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</div>
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<div class="portlet_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 unavailable round" title="Clinical test">C</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">Congenital hypertrophy of retinal pigment epithelium</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><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/870893" ref="tree=MeSH" title="MedGen record for Abnormal posterior eye segment morphology">Abnormal posterior eye segment morphology</a></span><ul><li><span class="TLline"><a href="/medgen/871316" ref="tree=MeSH" title="MedGen record for Abnormal fundus morphology">Abnormal fundus morphology</a></span><ul><li><span class="TLline"><a href="/medgen/1644580" ref="tree=MeSH" title="MedGen record for Abnormality of fundus pigmentation">Abnormality of fundus pigmentation</a></span><ul><li><span class="TLline"><a href="/medgen/866794" ref="tree=MeSH" title="MedGen record for Hyperpigmentation of the fundus">Hyperpigmentation of the fundus</a></span><ul><li><span class="matched_ds">Congenital hypertrophy of retinal pigment epithelium</span><ul><li><span class="TLline"><a href="/medgen/892829" ref="tree=MeSH" title="MedGen record for Grouped congenital hypertrophy of retinal pigment epithelium">Grouped congenital hypertrophy of retinal pigment epithelium</a></span></li><li><span class="TLline"><a href="/medgen/866792" ref="tree=MeSH" title="MedGen record for Multiple bilateral congenital hypertrophy of retinal pigment epithelium">Multiple bilateral congenital hypertrophy of retinal pigment epithelium</a></span></li><li><span class="TLline"><a href="/medgen/866793" ref="tree=MeSH" title="MedGen record for Solitary congenital hypertrophy of retinal pigment epithelium">Solitary congenital hypertrophy of retinal pigment epithelium</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
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||
<div class="portlet mgSection" id="ID_112">
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||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_398651"><div><strong>Familial adenomatous polyposis 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>398651</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.">C2713442</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">APC-associated polyposis conditions include (classic or attenuated) familial adenomatous polyposis (FAP) and gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS). FAP is a colorectal cancer (CRC) predisposition syndrome that can manifest in either classic or attenuated form. Classic FAP is characterized by hundreds to thousands of adenomatous colonic polyps, beginning on average at age 16 years (range 7-36 years). For those with the classic form of FAP, 95% of individuals have polyps by age 35 years; CRC is inevitable without colectomy. The mean age of CRC diagnosis in untreated individuals is 39 years (range 34-43 years). The attenuated form is characterized by multiple colonic polyps (average of 30), more proximally located polyps, and a diagnosis of CRC at a later age than in classic FAP. For those with an attenuated form, there is a 70% lifetime risk of CRC and the mean age of diagnosis is 50-55 years. Extracolonic manifestations are variably present and include polyps of the stomach and duodenum, osteomas, dental abnormalities, congenital hypertrophy of the retinal pigment epithelium (CHRPE), benign cutaneous lesions, desmoid tumors, adrenal masses, and other associated cancers. GAPPS is characterized by proximal gastric polyposis, increased risk of gastric adenocarcinoma, and no duodenal or colonic involvement in most individuals reported.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/398651">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_398651" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Familial adenomatous polyposis 1</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
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||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<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/12721244">Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bertario L,
|
||
Russo A,
|
||
Sala P,
|
||
Varesco L,
|
||
Giarola M,
|
||
Mondini P,
|
||
Pierotti M,
|
||
Spinelli P,
|
||
Radice P;
|
||
Hereditary Colorectal Tumor Registry</span><br />
|
||
<span class="medgenPMjournal">J Clin Oncol</span>
|
||
2003 May 1;21(9):1698-707.
|
||
doi: 10.1200/JCO.2003.09.118.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12721244" target="_blank">12721244</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22congenital%20hypertrophy%20of%20retinal%20pigment%20epithelium%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></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/35819078">Retinal Vascular Patterns and Capillary Plexus Reflectivity of Intraocular Tumors; an Optical Coherence Tomography Angiography Study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gönen B,
|
||
Hepokur M,
|
||
Güleser ÜY,
|
||
Yetik H,
|
||
Sarıcı AM</span><br />
|
||
<span class="medgenPMjournal">Curr Eye Res</span>
|
||
2022 Oct;47(10):1424-1435.
|
||
Epub 2022 Jul 25
|
||
doi: 10.1080/02713683.2022.2101666.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35819078" target="_blank">35819078</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29288030">Peripheral Pigmented Retinal Lesions in Stargardt Disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhao PY,
|
||
Abalem MF,
|
||
Nadelman D,
|
||
Qian CX,
|
||
Branham K,
|
||
Schlegel D,
|
||
Khan N,
|
||
Heckenlively JR,
|
||
Jayasundera T</span><br />
|
||
<span class="medgenPMjournal">Am J Ophthalmol</span>
|
||
2018 Apr;188:104-110.
|
||
Epub 2017 Dec 27
|
||
doi: 10.1016/j.ajo.2017.12.011.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29288030" target="_blank">29288030</a><a href="/pmc/articles/PMC5994923" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25326340">Congenital hypertrophy of retinal pigment epithelium (CHRPE) in patients with familial adenomatous polyposis (FAP); a polyposis registry experience.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nusliha A,
|
||
Dalpatadu U,
|
||
Amarasinghe B,
|
||
Chandrasinghe PC,
|
||
Deen KI</span><br />
|
||
<span class="medgenPMjournal">BMC Res Notes</span>
|
||
2014 Oct 18;7:734.
|
||
doi: 10.1186/1756-0500-7-734.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25326340" target="_blank">25326340</a><a href="/pmc/articles/PMC4210554" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11857735">Differential occurrence of mutations causative of eye diseases in the Chinese population.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pang CP,
|
||
Lam DS</span><br />
|
||
<span class="medgenPMjournal">Hum Mutat</span>
|
||
2002 Mar;19(3):189-208.
|
||
doi: 10.1002/humu.10053.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11857735" target="_blank">11857735</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10374435">Incidence and predictive value of congenital hypertrophy of retinal pigment epithelium in Chinese familial adenomatous polyposis patients.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lam DS,
|
||
Kwok SP,
|
||
Kwok AK,
|
||
Liew CT,
|
||
Lau JW,
|
||
Pang CC</span><br />
|
||
<span class="medgenPMjournal">Chin Med J (Engl)</span>
|
||
1998 Mar;111(3):278-81.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10374435" target="_blank">10374435</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Congenital%20hypertrophy%20of%20retinal%20pigment%20epithelium%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 (11)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34752306">OCT Angiography of Peripapillary Congenital Hypertrophy of Retinal Pigment Epithelium.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Özdemir HB,
|
||
Şekeroğlu MA</span><br />
|
||
<span class="medgenPMjournal">Ophthalmol Retina</span>
|
||
2021 Nov;5(11):1163.
|
||
doi: 10.1016/j.oret.2021.08.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34752306" target="_blank">34752306</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32971657">Multimodal imaging in circumpapillary congenital hypertrophy of retinal pigment epithelium.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shanmugam M,
|
||
Dubey D,
|
||
Ramanjulu R,
|
||
Mishra D</span><br />
|
||
<span class="medgenPMjournal">Indian J Ophthalmol</span>
|
||
2020 Oct;68(10):2232-2233.
|
||
doi: 10.4103/ijo.IJO_196_20.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32971657" target="_blank">32971657</a><a href="/pmc/articles/PMC7727979" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28541252">Congenital Hypertrophy of Retinal Pigment Epithelium With Overlying Thin Adenoma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pefkianaki M,
|
||
Mashayekhi A,
|
||
Shields JA,
|
||
Shields CL</span><br />
|
||
<span class="medgenPMjournal">Retina</span>
|
||
2017 Jun;37(6):e69-e70.
|
||
doi: 10.1097/IAE.0000000000001483.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28541252" target="_blank">28541252</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27853017">An unusual case of congenital hypertrophy of retinal pigment epithelium with overlying hemorrhages.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chawla R,
|
||
Temkar S,
|
||
Sagar P,
|
||
Venkatesh P</span><br />
|
||
<span class="medgenPMjournal">Indian J Ophthalmol</span>
|
||
2016 Sep;64(9):672-673.
|
||
doi: 10.4103/0301-4738.194333.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27853017" target="_blank">27853017</a><a href="/pmc/articles/PMC5151159" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26516253">Macular congenital hypertrophy of retinal pigment epithelium (CHRPE) in a patient with best vitelliform dystrophy (BVD).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kumar V,
|
||
Chandra P,
|
||
Kumar A</span><br />
|
||
<span class="medgenPMjournal">BMJ Case Rep</span>
|
||
2015 Oct 29;2015
|
||
doi: 10.1136/bcr-2015-212832.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26516253" target="_blank">26516253</a><a href="/pmc/articles/PMC4636695" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Congenital%20hypertrophy%20of%20retinal%20pigment%20epithelium%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 (22)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34511415">Rare presentation of choroidal neovascularisation in a case of congenital hypertrophy of retinal pigment epithelium.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Venkatesh R,
|
||
Reddy NG,
|
||
Pulipaka RS,
|
||
Pereira A</span><br />
|
||
<span class="medgenPMjournal">BMJ Case Rep</span>
|
||
2021 Sep 12;14(9)
|
||
doi: 10.1136/bcr-2021-244554.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34511415" target="_blank">34511415</a><a href="/pmc/articles/PMC8438746" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Congenital%20hypertrophy%20of%20retinal%20pigment%20epithelium%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 (1)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/25326340">Congenital hypertrophy of retinal pigment epithelium (CHRPE) in patients with familial adenomatous polyposis (FAP); a polyposis registry experience.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nusliha A,
|
||
Dalpatadu U,
|
||
Amarasinghe B,
|
||
Chandrasinghe PC,
|
||
Deen KI</span><br />
|
||
<span class="medgenPMjournal">BMC Res Notes</span>
|
||
2014 Oct 18;7:734.
|
||
doi: 10.1186/1756-0500-7-734.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25326340" target="_blank">25326340</a><a href="/pmc/articles/PMC4210554" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11857735">Differential occurrence of mutations causative of eye diseases in the Chinese population.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pang CP,
|
||
Lam DS</span><br />
|
||
<span class="medgenPMjournal">Hum Mutat</span>
|
||
2002 Mar;19(3):189-208.
|
||
doi: 10.1002/humu.10053.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11857735" target="_blank">11857735</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10374435">Incidence and predictive value of congenital hypertrophy of retinal pigment epithelium in Chinese familial adenomatous polyposis patients.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lam DS,
|
||
Kwok SP,
|
||
Kwok AK,
|
||
Liew CT,
|
||
Lau JW,
|
||
Pang CC</span><br />
|
||
<span class="medgenPMjournal">Chin Med J (Engl)</span>
|
||
1998 Mar;111(3):278-81.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10374435" target="_blank">10374435</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8661634">Screening by genomic linkage studies and mutation analysis of hereditary adenomatous polyposis coli: usefulness for clinical practice.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Karner-Hanusch J,
|
||
Wolf B,
|
||
Zehetmayer M,
|
||
Wrba F,
|
||
Roth E,
|
||
Mannhalter C</span><br />
|
||
<span class="medgenPMjournal">World J Surg</span>
|
||
1996 Jun;20(5):578-83; discussion 583-4.
|
||
doi: 10.1007/s002689900090.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8661634" target="_blank">8661634</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8381318">Congenital hypertrophy of retinal pigment epithelium (CHRPE) as a marker for familial adenomatous polyposis (FAP).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bertario L,
|
||
Bandello F,
|
||
Rossetti C,
|
||
Sala P,
|
||
Fortini E,
|
||
Spinelli P,
|
||
Gennari L,
|
||
Pietroiusti M,
|
||
Presciuttini S</span><br />
|
||
<span class="medgenPMjournal">Eur J Cancer Prev</span>
|
||
1993 Jan;2(1):69-75.
|
||
doi: 10.1097/00008469-199301000-00011.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8381318" target="_blank">8381318</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Congenital%20hypertrophy%20of%20retinal%20pigment%20epithelium%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 (5)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35819078">Retinal Vascular Patterns and Capillary Plexus Reflectivity of Intraocular Tumors; an Optical Coherence Tomography Angiography Study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gönen B,
|
||
Hepokur M,
|
||
Güleser ÜY,
|
||
Yetik H,
|
||
Sarıcı AM</span><br />
|
||
<span class="medgenPMjournal">Curr Eye Res</span>
|
||
2022 Oct;47(10):1424-1435.
|
||
Epub 2022 Jul 25
|
||
doi: 10.1080/02713683.2022.2101666.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35819078" target="_blank">35819078</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30900602">Ocular coherence tomography angiography features of congenital hypertrophy of retinal pigment epithelium.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shanmugam PM,
|
||
Konana VK,
|
||
Ramanjulu R,
|
||
Mishra KCD,
|
||
Sagar P,
|
||
Simakurthy S</span><br />
|
||
<span class="medgenPMjournal">Indian J Ophthalmol</span>
|
||
2019 Apr;67(4):563-566.
|
||
doi: 10.4103/ijo.IJO_801_18.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30900602" target="_blank">30900602</a><a href="/pmc/articles/PMC6446643" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25326340">Congenital hypertrophy of retinal pigment epithelium (CHRPE) in patients with familial adenomatous polyposis (FAP); a polyposis registry experience.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nusliha A,
|
||
Dalpatadu U,
|
||
Amarasinghe B,
|
||
Chandrasinghe PC,
|
||
Deen KI</span><br />
|
||
<span class="medgenPMjournal">BMC Res Notes</span>
|
||
2014 Oct 18;7:734.
|
||
doi: 10.1186/1756-0500-7-734.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25326340" target="_blank">25326340</a><a href="/pmc/articles/PMC4210554" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11296028">Adenocarcinoma arising from congenital hypertrophy of retinal pigment epithelium.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shields JA,
|
||
Shields CL,
|
||
Eagle RC Jr,
|
||
Singh AD</span><br />
|
||
<span class="medgenPMjournal">Arch Ophthalmol</span>
|
||
2001 Apr;119(4):597-602.
|
||
doi: 10.1001/archopht.119.4.597.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11296028" target="_blank">11296028</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10374435">Incidence and predictive value of congenital hypertrophy of retinal pigment epithelium in Chinese familial adenomatous polyposis patients.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lam DS,
|
||
Kwok SP,
|
||
Kwok AK,
|
||
Liew CT,
|
||
Lau JW,
|
||
Pang CC</span><br />
|
||
<span class="medgenPMjournal">Chin Med J (Engl)</span>
|
||
1998 Mar;111(3):278-81.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10374435" target="_blank">10374435</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Congenital%20hypertrophy%20of%20retinal%20pigment%20epithelium%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 (8)</a></div></div>
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