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<meta name="keywords" content="C4255215, congenital abnormality, congenital dysplasia of tricuspid valve, dysplastic tricuspid valve, tricuspid valvar dysplasia, tricuspid valve dysplasia, 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="A congenital malformation of the tricuspid valve characterized by leaflet deformation." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=901243
|
||
ConceptID=C4255215
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Dysplastic tricuspid valve</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>901243</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.">C4255215</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Congenital dysplasia of tricuspid valve; Tricuspid valvar dysplasia; Tricuspid valve dysplasia</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Congenital dysplasia of tricuspid valve (762254000); Tricuspid valvar dysplasia (762254000)</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:0030732">HP:0030732</a></td></tr>
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||
<div class="portlet_content ln">A congenital malformation of the tricuspid valve characterized by leaflet deformation. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet 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">Dysplastic tricuspid valve</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/116727" ref="tree=MeSH" title="MedGen record for Abnormality of the cardiovascular system">Abnormality of the cardiovascular system</a></span><ul><li><span class="TLline"><a href="/medgen/892473" ref="tree=MeSH" title="MedGen record for Abnormal cardiovascular system morphology">Abnormal cardiovascular system morphology</a></span><ul><li><span class="TLline"><a href="/medgen/6748" ref="tree=MeSH" title="MedGen record for Abnormal heart morphology">Abnormal heart morphology</a></span><ul><li><span class="TLline"><a href="/medgen/892837" ref="tree=MeSH" title="MedGen record for Abnormal heart valve morphology">Abnormal heart valve morphology</a></span><ul><li><span class="TLline"><a href="/medgen/870547" ref="tree=MeSH" title="MedGen record for Abnormal atrioventricular valve morphology">Abnormal atrioventricular valve morphology</a></span><ul><li><span class="TLline"><a href="/medgen/871267" ref="tree=MeSH" title="MedGen record for Abnormal tricuspid valve morphology">Abnormal tricuspid valve morphology</a></span><ul><li><span class="matched_ds">Dysplastic tricuspid valve</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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||
</div>
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<div class="portlet mgSection" id="ID_112">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln clinfeat">
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||
<div class="divPopper rprt" id="rdis_75567"><div><strong>CHARGE syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75567</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.">C0265354</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">CHD7 disorder encompasses the entire phenotypic spectrum of heterozygous CHD7 pathogenic variants that includes CHARGE syndrome as well as subsets of features that comprise the CHARGE syndrome phenotype. The mnemonic CHARGE syndrome, introduced in the premolecular era, stands for coloboma, heart defect, choanal atresia, retarded growth and development, genital hypoplasia, ear anomalies (including deafness). Following the identification of the genetic cause of CHD7 disorder, the phenotypic spectrum expanded to include cranial nerve anomalies, vestibular defects, cleft lip and/or palate, hypothyroidism, tracheoesophageal anomalies, brain anomalies, seizures, and renal anomalies. Life expectancy highly depends on the severity of manifestations; mortality can be high in the first few years when severe birth defects (particularly complex heart defects) are present and often complicated by airway and feeding issues. In childhood, adolescence, and adulthood, decreased life expectancy is likely related to a combination of residual heart defects, infections, aspiration or choking, respiratory issues including obstructive and central apnea, and possibly seizures. Despite these complications, the life expectancy for many individuals can be normal.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/75567">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_444060"><div><strong>Cardiospondylocarpofacial syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>444060</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.">C2931461</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Cardiospondylocarpofacial syndrome (CSCF) is characterized by growth retardation, dysmorphic facial features, brachydactyly with carpal-tarsal fusion, extensive posterior cervical vertebral synostosis, cardiac septal defects with valve dysplasia, and deafness with inner ear malformations (summary by Le Goff et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/444060">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_755478"><div><strong>Alveolar capillary dysplasia with pulmonary venous misalignment</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>755478</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.">C2960310</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Congenital alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV) is characterized histologically by failure of formation and ingrowth of alveolar capillaries that then do not make contact with alveolar epithelium, medial muscular thickening of small pulmonary arterioles with muscularization of the intraacinar arterioles, thickened alveolar walls, and anomalously situated pulmonary veins running alongside pulmonary arterioles and sharing the same adventitial sheath. Less common features include a reduced number of alveoli and a patchy distribution of the histopathologic changes. The disorder is associated with persistent pulmonary hypertension of the neonate and shows varying degrees of lability and severity (Boggs et al., 1994). Affected infants present with respiratory distress resulting from pulmonary hypertension in the early postnatal period, and the disease is uniformly fatal within the newborn period (Vassal et al., 1998). Additional features of ACDMPV include multiple congenital anomalies affecting the cardiovascular, gastrointestinal, genitourinary, and musculoskeletal systems, as well as disruption of the normal right-left asymmetry of intrathoracic or intraabdominal organs (Sen et al., 2004).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/755478">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_461565"><div><strong>Chromosome 6q24-q25 deletion syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>461565</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.">C3150215</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">6q25 microdeletion syndrome is a recently described syndrome characterized by developmental delay, facial dysmorphism and hearing loss.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/461565">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1648333"><div><strong>Cardiac-urogenital syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1648333</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.">C4748946</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">MYRF-related cardiac urogenital syndrome (MYRF-CUGS) is primarily characterized by anomalies of the internal and external genitalia, congenital heart defects, and eye anomalies. 46,XY individuals can have a range of anomalies of the genitalia, from isolated unilateral cryptorchidism to ambiguous genitalia to typical-appearing female genitalia. 46,XX individuals can have atypical internal genitalia including absent uterus, absent fallopian tubes, small or absent ovaries, absent vagina, or blind-ending vagina. A number of congenital heart defects have been described, with scimitar syndrome being the most common. Eye issues, present in a vast majority of affected individuals, include high hyperopia and nanophthalmos (an ocular malformation featuring short axial length due to small anterior and posterior segments with thickened choroid and sclera and normal lens volume). Because of the common nature of the eye anomalies, it has been suggested that this condition may be more accurately referred to as "MYRF-related ocular cardiac urogenital syndrome." Other features of the condition include a broad range of developmental delay /intellectual disability (DD/ID), from typical development and cognition to severe DD/ID; pulmonary abnormalities and diaphragmatic issues (congenital diaphragmatic hernia / diaphragmatic eventration); intestinal malrotation; and mild growth and feeding problems.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1648333">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_755478" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Alveolar capillary dysplasia with pulmonary venous misalignment</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1648333" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cardiac-urogenital syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_444060" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cardiospondylocarpofacial syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_75567" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">CHARGE syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_461565" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Chromosome 6q24-q25 deletion syndrome</a></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/19492249">Percutaneous balloon valvuloplasty for the treatment of pulmonary valve stenosis in children - a single centre experience.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Weryński P,
|
||
Rudziński A,
|
||
Król-Jawień W,
|
||
Kuźma J</span><br />
|
||
<span class="medgenPMjournal">Kardiol Pol</span>
|
||
2009 Apr;67(4):369-75.
|
||
<span class="bold">PMID: </span><a href="/pubmed/19492249" target="_blank">19492249</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18765936">Fetal cardiac diagnosis and its influence on the pregnancy and newborn--a tertiary centre experience.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Yeu BK,
|
||
Chalmers R,
|
||
Shekleton P,
|
||
Grimwade J,
|
||
Menahem S</span><br />
|
||
<span class="medgenPMjournal">Fetal Diagn Ther</span>
|
||
2008;24(3):241-5.
|
||
Epub 2008 Sep 2
|
||
doi: 10.1159/000151669.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18765936" target="_blank">18765936</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(dysplastic%20tricuspid%20valve)%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 (2)</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/25736309">BNP and haematological parameters are markers of severity of Ebstein's anomaly: correlation with CMR and cardiopulmonary exercise testing.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hösch O,
|
||
Ngyuen TT,
|
||
Lauerer P,
|
||
Schuster A,
|
||
Kutty S,
|
||
Staab W,
|
||
Unterberg-Buchwald C,
|
||
Sohns JM,
|
||
Paul T,
|
||
Lotz J,
|
||
Steinmetz M</span><br />
|
||
<span class="medgenPMjournal">Eur Heart J Cardiovasc Imaging</span>
|
||
2015 Jun;16(6):670-5.
|
||
Epub 2015 Mar 2
|
||
doi: 10.1093/ehjci/jeu312.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25736309" target="_blank">25736309</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23489067">Giant right atrium due to congenital dysplastic tricuspid valve in an elderly female patient.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shankarappa RK,
|
||
Papaiah S,
|
||
Karur S,
|
||
Math RS,
|
||
Nanjappa MC</span><br />
|
||
<span class="medgenPMjournal">Echocardiography</span>
|
||
2013 May;30(5):E128-31.
|
||
Epub 2013 Mar 12
|
||
doi: 10.1111/echo.12160.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23489067" target="_blank">23489067</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16784078">Repair of a dysplastic tricuspid valve using artificial chordae: case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Honjo O,
|
||
Ishino K,
|
||
Yoshizumi K,
|
||
Kawada M,
|
||
Ohtsuki S,
|
||
Akagi T,
|
||
Sano S</span><br />
|
||
<span class="medgenPMjournal">J Heart Valve Dis</span>
|
||
2006 May;15(3):392-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16784078" target="_blank">16784078</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Dysplastic%20tricuspid%20valve%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 (3)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/24809365">Atypical atrioventricular nodal reentry tachycardia in a child with polyvalvular dysplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Johnson JN,
|
||
Ackerman MJ,
|
||
Cannon BC</span><br />
|
||
<span class="medgenPMjournal">Cardiol Young</span>
|
||
2015 Mar;25(3):584-7.
|
||
Epub 2014 May 9
|
||
doi: 10.1017/S1047951114000717.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24809365" target="_blank">24809365</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25540215">Idiopathic aneurysmal giant right atrial enlargement with thrombus formation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Khare R,
|
||
Chandra S,
|
||
Agarwal V,
|
||
Dwivedi S</span><br />
|
||
<span class="medgenPMjournal">BMJ Case Rep</span>
|
||
2014 Dec 24;2014
|
||
doi: 10.1136/bcr-2014-207559.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25540215" target="_blank">25540215</a><a href="/pmc/articles/PMC4281571" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23489067">Giant right atrium due to congenital dysplastic tricuspid valve in an elderly female patient.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shankarappa RK,
|
||
Papaiah S,
|
||
Karur S,
|
||
Math RS,
|
||
Nanjappa MC</span><br />
|
||
<span class="medgenPMjournal">Echocardiography</span>
|
||
2013 May;30(5):E128-31.
|
||
Epub 2013 Mar 12
|
||
doi: 10.1111/echo.12160.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23489067" target="_blank">23489067</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10556393">Successful management of severe tricuspid regurgitation associated with hydrops fetalis in a case of dysplastic tricuspid valve.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Misu Y,
|
||
Hiraishi S,
|
||
Oguchi K,
|
||
Amano K</span><br />
|
||
<span class="medgenPMjournal">Pediatr Cardiol</span>
|
||
1999 Nov-Dec;20(6):435-7.
|
||
doi: 10.1007/s002469900508.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10556393" target="_blank">10556393</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9370403">The morphologically tricuspid valve in hypoplastic left heart syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Stamm C,
|
||
Anderson RH,
|
||
Ho SY</span><br />
|
||
<span class="medgenPMjournal">Eur J Cardiothorac Surg</span>
|
||
1997 Oct;12(4):587-92.
|
||
doi: 10.1016/s1010-7940(97)00184-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9370403" target="_blank">9370403</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Dysplastic%20tricuspid%20valve%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 (13)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/20449712">Radical surgery for a ventricular septal defect associated with trisomy 18.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kobayashi J,
|
||
Kaneko Y,
|
||
Yamamoto Y,
|
||
Yoda H,
|
||
Tsuchiya K</span><br />
|
||
<span class="medgenPMjournal">Gen Thorac Cardiovasc Surg</span>
|
||
2010 May;58(5):223-7.
|
||
Epub 2010 May 7
|
||
doi: 10.1007/s11748-009-0431-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20449712" target="_blank">20449712</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10556393">Successful management of severe tricuspid regurgitation associated with hydrops fetalis in a case of dysplastic tricuspid valve.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Misu Y,
|
||
Hiraishi S,
|
||
Oguchi K,
|
||
Amano K</span><br />
|
||
<span class="medgenPMjournal">Pediatr Cardiol</span>
|
||
1999 Nov-Dec;20(6):435-7.
|
||
doi: 10.1007/s002469900508.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10556393" target="_blank">10556393</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8914786">Severe right heart failure in a patient with Grave's disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Xenopoulos NP,
|
||
Braden GA,
|
||
Applegate RJ</span><br />
|
||
<span class="medgenPMjournal">Clin Cardiol</span>
|
||
1996 Nov;19(11):903-5.
|
||
doi: 10.1002/clc.4960191113.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8914786" target="_blank">8914786</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Dysplastic%20tricuspid%20valve%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 (3)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39326393">Double Outlet Left Ventricle with Intact Ventricular Septum: A Rare Prenatally Diagnosed Case Report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gur J,
|
||
Collins MP,
|
||
Smith F,
|
||
Tague L</span><br />
|
||
<span class="medgenPMjournal">Fetal Diagn Ther</span>
|
||
2025;52(1):19-23.
|
||
Epub 2024 Sep 26
|
||
doi: 10.1159/000541164.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39326393" target="_blank">39326393</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25736309">BNP and haematological parameters are markers of severity of Ebstein's anomaly: correlation with CMR and cardiopulmonary exercise testing.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hösch O,
|
||
Ngyuen TT,
|
||
Lauerer P,
|
||
Schuster A,
|
||
Kutty S,
|
||
Staab W,
|
||
Unterberg-Buchwald C,
|
||
Sohns JM,
|
||
Paul T,
|
||
Lotz J,
|
||
Steinmetz M</span><br />
|
||
<span class="medgenPMjournal">Eur Heart J Cardiovasc Imaging</span>
|
||
2015 Jun;16(6):670-5.
|
||
Epub 2015 Mar 2
|
||
doi: 10.1093/ehjci/jeu312.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25736309" target="_blank">25736309</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20449712">Radical surgery for a ventricular septal defect associated with trisomy 18.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kobayashi J,
|
||
Kaneko Y,
|
||
Yamamoto Y,
|
||
Yoda H,
|
||
Tsuchiya K</span><br />
|
||
<span class="medgenPMjournal">Gen Thorac Cardiovasc Surg</span>
|
||
2010 May;58(5):223-7.
|
||
Epub 2010 May 7
|
||
doi: 10.1007/s11748-009-0431-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20449712" target="_blank">20449712</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16784078">Repair of a dysplastic tricuspid valve using artificial chordae: case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Honjo O,
|
||
Ishino K,
|
||
Yoshizumi K,
|
||
Kawada M,
|
||
Ohtsuki S,
|
||
Akagi T,
|
||
Sano S</span><br />
|
||
<span class="medgenPMjournal">J Heart Valve Dis</span>
|
||
2006 May;15(3):392-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16784078" target="_blank">16784078</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10404462">Neonatal Marfan syndrome: a case report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ng DK,
|
||
Chau KW,
|
||
Black C,
|
||
Thomas TM,
|
||
Mak KL,
|
||
Boxer M</span><br />
|
||
<span class="medgenPMjournal">J Paediatr Child Health</span>
|
||
1999 Jun;35(3):321-3.
|
||
doi: 10.1046/j.1440-1754.1999.00355.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10404462" target="_blank">10404462</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Dysplastic%20tricuspid%20valve%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 (6)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39326393">Double Outlet Left Ventricle with Intact Ventricular Septum: A Rare Prenatally Diagnosed Case Report.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gur J,
|
||
Collins MP,
|
||
Smith F,
|
||
Tague L</span><br />
|
||
<span class="medgenPMjournal">Fetal Diagn Ther</span>
|
||
2025;52(1):19-23.
|
||
Epub 2024 Sep 26
|
||
doi: 10.1159/000541164.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39326393" target="_blank">39326393</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Dysplastic%20tricuspid%20valve%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 (1)</a></div></div>
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