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<meta name="keywords" content="C0034895, abnormal connection between rectum and vagina, anatomical abnormality, finding, fistula, rectovaginal, fistulas, rectovaginal, rectovaginal fistula, rectovaginal fistulas, rvf - rectovaginal fistula, 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="The presence of a fistula between the vagina and the rectum." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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||
UID=11152
|
||
ConceptID=C0034895
|
||
-->
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||
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Rectovaginal fistula</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>11152</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.">C0034895</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Anatomical Abnormality; Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Fistula, Rectovaginal; Fistulas, Rectovaginal; Rectovaginal Fistula; Rectovaginal Fistulas</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Rectovaginal fistula (65619001); RVF - Rectovaginal fistula (65619001)</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:0000143">HP:0000143</a></td></tr>
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</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>
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<div class="portlet mgSection" id="ID_100">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">The presence of a fistula between the vagina and the rectum. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
|
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</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0034895[DISCUI]&test_type=Clinical&redirect=true" ref="ncbi_uid=11152">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Rectovaginal fistula</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/4347" ref="tree=MeSH" title="MedGen record for Disease">Disease</a></span><ul><li><span class="TLline"><a href="/medgen/311052" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Disorder">Non-Neoplastic Disorder</a></span><ul><li><span class="TLline"><a href="/medgen/317955" ref="tree=MeSH" title="MedGen record for Non-Neoplastic Disorder by Special Category">Non-Neoplastic Disorder by Special Category</a></span><ul><li><span class="TLline"><a href="/medgen/90143" ref="tree=MeSH" title="MedGen record for Deformity">Deformity</a></span><ul><li><span class="TLline"><a href="/medgen/5201" ref="tree=MeSH" title="MedGen record for Sinus">Sinus</a></span><ul><li><span class="TLline"><a href="/medgen/82841" ref="tree=MeSH" title="MedGen record for Fistula of the female genital organs">Fistula of the female genital organs</a></span><ul><li><span class="matched_ds">Rectovaginal fistula</span></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">
|
||
<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_59798"><div><strong>Johanson-Blizzard syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>59798</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.">C0175692</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Johanson-Blizzard syndrome (JBS) is an autosomal recessive disorder characterized by poor growth, impaired intellectual development, and variable dysmorphic features, including aplasia or hypoplasia of the nasal alae, abnormal hair patterns or scalp defects, and oligodontia. Other features include hypothyroidism, sensorineural hearing loss, imperforate anus, and pancreatic exocrine insufficiency (summary by Al-Dosari et al., 2008).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/59798">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_120532"><div><strong>Baller-Gerold syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>120532</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.">C0265308</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Baller-Gerold syndrome (BGS) can be suspected at birth in an infant with craniosynostosis and upper limb abnormality. The coronal suture is most commonly affected; the metopic, lambdoid, and sagittal sutures may also be involved alone or in combination. Upper limb abnormality can include a combination of thumb hypo- or aplasia and radial hypo- or aplasia and may be asymmetric. Malformation or absence of carpal or metacarpal bones has also been described. Skin lesions may appear anytime within the first few years after birth, typically beginning with erythema of the face and extremities and evolving into poikiloderma. Slow growth is apparent in infancy with eventual height and length typically at 4 SD below the mean.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/120532">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_162915"><div><strong>Acrocallosal syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>162915</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.">C0796147</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Classic Joubert syndrome (JS) is characterized by three primary findings: A distinctive cerebellar and brain stem malformation called the molar tooth sign (MTS). Hypotonia. Developmental delays. Often these findings are accompanied by episodic tachypnea or apnea and/or atypical eye movements. In general, the breathing abnormalities improve with age, truncal ataxia develops over time, and acquisition of gross motor milestones is delayed. Cognitive abilities are variable, ranging from severe intellectual disability to normal. Additional findings can include retinal dystrophy, renal disease, ocular colobomas, occipital encephalocele, hepatic fibrosis, polydactyly, oral hamartomas, and endocrine abnormalities. Both intra- and interfamilial variation are seen.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/162915">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_184924"><div><strong>McKusick-Kaufman syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>184924</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.">C0948368</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">McKusick-Kaufman syndrome (MKS) is characterized by the combination of postaxial polydactyly (PAP), congenital heart disease (CHD), and hydrometrocolpos (HMC) in females and genital malformations in males (most commonly hypospadias, cryptorchidism, and chordee). HMC in infants usually presents as a large cystic abdominal mass arising out of the pelvis, caused by dilatation of the vagina and uterus as a result of the accumulation of cervical secretions from maternal estrogen stimulation. HMC can be caused by failure of the distal third of the vagina to develop (vaginal agenesis), a transverse vaginal membrane, or an imperforate hymen. PAP is the presence of additional digits on the ulnar side of the hand and the fibular side of the foot. A variety of congenital heart defects have been reported including atrioventricular canal, atrial septal defect, ventricular septal defect, or a complex congenital heart malformation.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/184924">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_233003"><div><strong>Oculootoradial syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>233003</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.">C1327918</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">IVIC syndrome (IVIC) is an autosomal dominant disorder characterized by upper limb anomalies (radial ray defects, carpal bone fusion), extraocular motor disturbances, and congenital bilateral nonprogressive mixed hearing loss. More variable features include heart involvement, mild thrombocytopenia and leukocytosis (before age 50), shoulder girdle hypoplasia, imperforate anus, kidney malrotation, and rectovaginal fistula (summary by Paradisi and Arias, 2007).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/233003">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_323460"><div><strong>Currarino triad</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>323460</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.">C1531773</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The Currarino syndrome is an autosomal dominant form of hereditary sacral dysgenesis that classically consists of the triad of sacral malformation, presacral mass, and anorectal malformations. However, other features include neonatal-onset bowel obstruction, chronic constipation, recurrent perianal sepsis, renal/urinary tract anomalies, female internal genital anomalies, tethered spinal cord, and anterior meningocele. There is marked inter- and intrafamilial variability, and up to 33% of patients are asymptomatic (summary by Wang et al., 2006).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/323460">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_333031"><div><strong>CODAS syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>333031</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.">C1838180</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">CODAS is an acronym for cerebral, ocular, dental, auricular, and skeletal anomalies. CODAS syndrome is a rare disorder characterized by a distinctive constellation of features that includes developmental delay, craniofacial anomalies, cataracts, ptosis, median nasal groove, delayed tooth eruption, hearing loss, short stature, delayed epiphyseal ossification, metaphyseal hip dysplasia, and vertebral coronal clefts (summary by Strauss et al., 2015).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/333031">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_338020"><div><strong>Exstrophy-epispadias complex</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>338020</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.">C1850321</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Carey et al. (1978) gave the name OEIS complex to a combination of defects comprising omphalocele, exstrophy of the cloaca, imperforate anus, and spinal defects. This rare complex is thought to represent the most severe end of a spectrum of birth defects, the exstrophy-epispadias sequence, which, in order of increasing severity, includes phallic separation with epispadias, pubic diastasis, exstrophy of the bladder (600057), cloacal exstrophy, and OEIS complex. Very few instances of recurrence of anomalies in this cluster have been reported.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/338020">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_343663"><div><strong>Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>343663</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.">C1851841</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">An EEC syndrome characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 7q11.2-q21.3.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/343663">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_351066"><div><strong>Craniosynostosis-anal anomalies-porokeratosis syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>351066</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.">C1864186</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">CDAGS syndrome is characterized by craniosynostosis and clavicular hypoplasia, delayed closure of the fontanel, anal and genitourinary anomalies, and skin eruption of porokeratotic lesions (Mendoza-Londono et al., 2005).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/351066">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_393403"><div><strong>Inflammatory bowel disease 25</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>393403</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.">C2675508</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Any inflammatory bowel disease in which the cause of the disease is a mutation in the IL10RB gene.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/393403">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_394424"><div><strong>Syndactyly-telecanthus-anogenital and renal malformations syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>394424</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.">C2678045</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Syndrome with the association of toe syndactyly, facial dysmorphism including telecanthus and a broad nasal tip, urogenital malformations and anal atresia. Around ten cases have been reported so far. The syndrome is caused by mutations in the FAM58A gene (located on the X chromosome) encoding a protein of unknown function.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/394424">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_413305"><div><strong>BNAR syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>413305</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.">C2750433</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">FREM1 autosomal recessive disorders include Manitoba oculotrichoanal (MOTA) syndrome, bifid nose with or without anorectal and renal anomalies (BNAR syndrome), and isolated congenital anomalies of kidney and urinary tract (CAKUT). MOTA syndrome is characterized by an aberrant hairline (unilateral or bilateral wedge-shaped extension of the anterior hairline from the temple region to the ipsilateral eye) and anomalies of the eyes (widely spaced eyes, anophthalmia/microphthalmia and/or cryptophthalmos, colobomas of the upper eyelid, and corneopalpebral synechiae), nose (bifid or broad nasal tip), abdominal wall (omphalocele or umbilical hernia), and anus (stenosis and/or anterior displacement of the anal opening). The manifestations and degree of severity vary even among affected members of the same family. Growth and psychomotor development are normal. BNAR syndrome is characterized by a bifid or wide nasal tip, anorectal anomalies, and renal malformations (e.g., renal agenesis, renal dysplasia). Typically the eye manifestations of MOTA syndrome are absent. FREM1-CAKUT was identified in one individual with bilateral vesicoureteral reflux (VUR) and a second individual with VUR and renal hypodysplasia.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/413305">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_501217"><div><strong>Anorectal anomaly</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>501217</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.">C3495676</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Anatomical Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">An abnormality of the anus or rectum.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/501217">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1381939"><div><strong>Townes-Brocks syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1381939</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.">C4479534</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1381939">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1635275"><div><strong>Townes-Brocks syndrome 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1635275</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.">C4551481</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">SALL1-related Townes-Brocks syndrome (SALL1-TBS) is characterized by the triad of imperforate anus or anal stenosis, dysplastic ears (overfolded superior helices and preauricular tags; frequently associated with sensorineural and/or conductive hearing impairment), and thumb malformations (duplication of the thumb [preaxial polydactyly], triphalangeal thumbs, and, rarely, hypoplasia of the thumbs) without hypoplasia of the radius. Impaired kidney function, including end-stage kidney disease (ESKD), may occur with or without structural abnormalities (mild malrotation, ectopia, horseshoe kidney, renal hypoplasia, polycystic kidneys, vesicoureteral reflux). Foot malformations (flat feet, overlapping toes) and genitourinary malformations are common. Congenital heart disease occurs in 15% of affected individuals. Developmental delay and/or learning difficulties occur in approximately 15% of affected individuals. Rare features include growth deficiency, Duane anomaly, iris coloboma, and Chiari I malformation.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1635275">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1778108"><div><strong>Congenital secretory sodium diarrhea 3</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1778108</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.">C5441927</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Any secretory diarrhea in which the cause of the disease is a mutation in the SPINT2 gene.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1778108">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1785087"><div><strong>White-Kernohan syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1785087</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.">C5543635</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">White-Kernohan syndrome (WHIKERS) is a neurodevelopmental disorder characterized by global developmental delay with variably impaired intellectual development, hypotonia, and characteristic facial features. Some patients may have abnormalities of other systems, including genitourinary and skeletal (summary by White et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1785087">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1811526"><div><strong>Gastrointestinal defects and immunodeficiency syndrome 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1811526</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.">C5676901</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">PI4KA-related disorder is a clinically variable disorder characterized primarily by neurologic dysfunction (limb spasticity, developmental delay, intellectual disability, seizures, ataxia, nystagmus), gastrointestinal manifestations (multiple intestinal atresia, inflammatory bowel disease), and combined immunodeficiency (leukopenia, variable immunoglobulin defects). Age of onset is typically antenatal or in early childhood; individuals can present with any combination of these features. Rare individuals present with later-onset hereditary spastic paraplegia. Brain MRI findings can include hypomyelinating leukodystrophy, cerebellar hypoplasia/atrophy, thin or dysplastic corpus callosum, and/or perisylvian polymicrogyria.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1811526">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_162915" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Acrocallosal syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_501217" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Anorectal anomaly</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_120532" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Baller-Gerold syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_413305" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">BNAR syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_333031" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">CODAS syndrome</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (19)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1778108" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Congenital secretory sodium diarrhea 3</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_351066" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Craniosynostosis-anal anomalies-porokeratosis syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_323460" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Currarino triad</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_343663" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_338020" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Exstrophy-epispadias complex</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1811526" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Gastrointestinal defects and immunodeficiency syndrome 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_393403" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Inflammatory bowel disease 25</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_59798" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Johanson-Blizzard syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_184924" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">McKusick-Kaufman syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_233003" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Oculootoradial syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_394424" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Syndactyly-telecanthus-anogenital and renal malformations syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1635275" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Townes-Brocks syndrome 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1381939" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Townes-Brocks syndrome 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1785087" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">White-Kernohan syndrome</a></div></span></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35732009">The American Society of Colon and Rectal Surgeons Clinical Practice Guidelines for the Management of Anorectal Abscess, Fistula-in-Ano, and Rectovaginal Fistula.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gaertner WB,
|
||
Burgess PL,
|
||
Davids JS,
|
||
Lightner AL,
|
||
Shogan BD,
|
||
Sun MY,
|
||
Steele SR,
|
||
Paquette IM,
|
||
Feingold DL;
|
||
Clinical Practice Guidelines Committee of the American Society of Colon and Rectal Surgeons</span><br />
|
||
<span class="medgenPMjournal">Dis Colon Rectum</span>
|
||
2022 Aug 1;65(8):964-985.
|
||
Epub 2022 Jul 5
|
||
doi: 10.1097/DCR.0000000000002473.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35732009" target="_blank">35732009</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34718590">Successful Treatment of Ulcerative Colitis, Rectovaginal Fistula, and Skin Erythema Nodule With Adalimumab.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dai C,
|
||
Huang YH,
|
||
Jiang M</span><br />
|
||
<span class="medgenPMjournal">Inflamm Bowel Dis</span>
|
||
2022 Mar 2;28(3):e36-e37.
|
||
doi: 10.1093/ibd/izab260.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34718590" target="_blank">34718590</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27824697">Clinical Practice Guideline for the Management of Anorectal Abscess, Fistula-in-Ano, and Rectovaginal Fistula.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vogel JD,
|
||
Johnson EK,
|
||
Morris AM,
|
||
Paquette IM,
|
||
Saclarides TJ,
|
||
Feingold DL,
|
||
Steele SR</span><br />
|
||
<span class="medgenPMjournal">Dis Colon Rectum</span>
|
||
2016 Dec;59(12):1117-1133.
|
||
doi: 10.1097/DCR.0000000000000733.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27824697" target="_blank">27824697</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22rectovaginal%20fistula%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 (53)</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/30824210">Choosing the right technique for deep endometriosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nisolle M,
|
||
Brichant G,
|
||
Tebache L</span><br />
|
||
<span class="medgenPMjournal">Best Pract Res Clin Obstet Gynaecol</span>
|
||
2019 Aug;59:56-65.
|
||
Epub 2019 Jan 29
|
||
doi: 10.1016/j.bpobgyn.2019.01.010.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30824210" target="_blank">30824210</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12516853">Rectovaginal fistula.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Saclarides TJ</span><br />
|
||
<span class="medgenPMjournal">Surg Clin North Am</span>
|
||
2002 Dec;82(6):1261-72.
|
||
doi: 10.1016/s0039-6109(02)00055-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12516853" target="_blank">12516853</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10707712">Rectal duplication.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kulkarni B,
|
||
Oak SN,
|
||
Karmarkar SJ,
|
||
Desai AP,
|
||
Deshmukh SS</span><br />
|
||
<span class="medgenPMjournal">J Postgrad Med</span>
|
||
1995 Apr-Jun;41(2):49-51.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10707712" target="_blank">10707712</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1775854">Metronidazole-induced acute pancreatitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Corey WA,
|
||
Doebbeling BN,
|
||
DeJong KJ,
|
||
Britigan BE</span><br />
|
||
<span class="medgenPMjournal">Rev Infect Dis</span>
|
||
1991 Nov-Dec;13(6):1213-5.
|
||
doi: 10.1093/clinids/13.6.1213.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1775854" target="_blank">1775854</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/876530">Cloacal dysgenesis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Okonkwo JE,
|
||
Crocker KM</span><br />
|
||
<span class="medgenPMjournal">Obstet Gynecol</span>
|
||
1977 Jul;50(1):97-101.
|
||
<span class="bold">PMID: </span><a href="/pubmed/876530" target="_blank">876530</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Rectovaginal%20fistula%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 (684)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/27824697">Clinical Practice Guideline for the Management of Anorectal Abscess, Fistula-in-Ano, and Rectovaginal Fistula.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Vogel JD,
|
||
Johnson EK,
|
||
Morris AM,
|
||
Paquette IM,
|
||
Saclarides TJ,
|
||
Feingold DL,
|
||
Steele SR</span><br />
|
||
<span class="medgenPMjournal">Dis Colon Rectum</span>
|
||
2016 Dec;59(12):1117-1133.
|
||
doi: 10.1097/DCR.0000000000000733.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27824697" target="_blank">27824697</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20109633">Rectovaginal fistula.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Champagne BJ,
|
||
McGee MF</span><br />
|
||
<span class="medgenPMjournal">Surg Clin North Am</span>
|
||
2010 Feb;90(1):69-82, Table of Contents.
|
||
doi: 10.1016/j.suc.2009.09.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20109633" target="_blank">20109633</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10707712">Rectal duplication.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kulkarni B,
|
||
Oak SN,
|
||
Karmarkar SJ,
|
||
Desai AP,
|
||
Deshmukh SS</span><br />
|
||
<span class="medgenPMjournal">J Postgrad Med</span>
|
||
1995 Apr-Jun;41(2):49-51.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10707712" target="_blank">10707712</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7985071">Anovaginal fistulae.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Senatore PJ Jr</span><br />
|
||
<span class="medgenPMjournal">Surg Clin North Am</span>
|
||
1994 Dec;74(6):1361-75.
|
||
doi: 10.1016/s0039-6109(16)46487-x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7985071" target="_blank">7985071</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/876530">Cloacal dysgenesis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Okonkwo JE,
|
||
Crocker KM</span><br />
|
||
<span class="medgenPMjournal">Obstet Gynecol</span>
|
||
1977 Jul;50(1):97-101.
|
||
<span class="bold">PMID: </span><a href="/pubmed/876530" target="_blank">876530</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Rectovaginal%20fistula%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 (350)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34718590">Successful Treatment of Ulcerative Colitis, Rectovaginal Fistula, and Skin Erythema Nodule With Adalimumab.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dai C,
|
||
Huang YH,
|
||
Jiang M</span><br />
|
||
<span class="medgenPMjournal">Inflamm Bowel Dis</span>
|
||
2022 Mar 2;28(3):e36-e37.
|
||
doi: 10.1093/ibd/izab260.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34718590" target="_blank">34718590</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21349773">Vaginal route: a gynaecological route for much more than hysterectomy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sheth SS,
|
||
Paghdiwalla KP,
|
||
Hajari AR</span><br />
|
||
<span class="medgenPMjournal">Best Pract Res Clin Obstet Gynaecol</span>
|
||
2011 Apr;25(2):115-32.
|
||
Epub 2011 Feb 23
|
||
doi: 10.1016/j.bpobgyn.2010.12.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21349773" target="_blank">21349773</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20109633">Rectovaginal fistula.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Champagne BJ,
|
||
McGee MF</span><br />
|
||
<span class="medgenPMjournal">Surg Clin North Am</span>
|
||
2010 Feb;90(1):69-82, Table of Contents.
|
||
doi: 10.1016/j.suc.2009.09.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20109633" target="_blank">20109633</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1775854">Metronidazole-induced acute pancreatitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Corey WA,
|
||
Doebbeling BN,
|
||
DeJong KJ,
|
||
Britigan BE</span><br />
|
||
<span class="medgenPMjournal">Rev Infect Dis</span>
|
||
1991 Nov-Dec;13(6):1213-5.
|
||
doi: 10.1093/clinids/13.6.1213.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1775854" target="_blank">1775854</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3318313">Rectovaginal fistula.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Stern HS,
|
||
Dreznik Z</span><br />
|
||
<span class="medgenPMjournal">Adv Surg</span>
|
||
1988;21:245-62.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3318313" target="_blank">3318313</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Rectovaginal%20fistula%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 (485)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32841755">Surgical Outcomes after Colorectal Surgery for Endometriosis: A Systematic Review and Meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bendifallah S,
|
||
Puchar A,
|
||
Vesale E,
|
||
Moawad G,
|
||
Daraï E,
|
||
Roman H</span><br />
|
||
<span class="medgenPMjournal">J Minim Invasive Gynecol</span>
|
||
2021 Mar;28(3):453-466.
|
||
Epub 2020 Aug 22
|
||
doi: 10.1016/j.jmig.2020.08.015.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32841755" target="_blank">32841755</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11137690">Advances in the management of anorectal malformations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Peña A,
|
||
Hong A</span><br />
|
||
<span class="medgenPMjournal">Am J Surg</span>
|
||
2000 Nov;180(5):370-6.
|
||
doi: 10.1016/s0002-9610(00)00491-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11137690" target="_blank">11137690</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10707712">Rectal duplication.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kulkarni B,
|
||
Oak SN,
|
||
Karmarkar SJ,
|
||
Desai AP,
|
||
Deshmukh SS</span><br />
|
||
<span class="medgenPMjournal">J Postgrad Med</span>
|
||
1995 Apr-Jun;41(2):49-51.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10707712" target="_blank">10707712</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/2296422">Early repair of episiotomy dehiscence.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hankins GD,
|
||
Hauth JC,
|
||
Gilstrap LC 3rd,
|
||
Hammond TL,
|
||
Yeomans ER,
|
||
Snyder RR</span><br />
|
||
<span class="medgenPMjournal">Obstet Gynecol</span>
|
||
1990 Jan;75(1):48-51.
|
||
<span class="bold">PMID: </span><a href="/pubmed/2296422" target="_blank">2296422</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/876530">Cloacal dysgenesis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Okonkwo JE,
|
||
Crocker KM</span><br />
|
||
<span class="medgenPMjournal">Obstet Gynecol</span>
|
||
1977 Jul;50(1):97-101.
|
||
<span class="bold">PMID: </span><a href="/pubmed/876530" target="_blank">876530</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Rectovaginal%20fistula%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 (359)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35779081">Surgical treatment of rectovaginal fistula-predictors of outcome and effects on quality of life.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Söderqvist EV,
|
||
Cashin PH,
|
||
Graf W</span><br />
|
||
<span class="medgenPMjournal">Int J Colorectal Dis</span>
|
||
2022 Jul;37(7):1699-1707.
|
||
Epub 2022 Jul 2
|
||
doi: 10.1007/s00384-022-04206-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35779081" target="_blank">35779081</a><a href="/pmc/articles/PMC9262790" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35332647">Postoperative rectovaginal fistula: Can colonic pull-through delayed coloanal anastomosis avoid the need for definitive stoma? An experience of 28 consecutives cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Blondeau M,
|
||
Labiad C,
|
||
Melka D,
|
||
de Ponthaud C,
|
||
Giacca M,
|
||
Monsinjon M,
|
||
Panis Y</span><br />
|
||
<span class="medgenPMjournal">Colorectal Dis</span>
|
||
2022 Aug;24(8):1000-1006.
|
||
Epub 2022 Apr 6
|
||
doi: 10.1111/codi.16124.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35332647" target="_blank">35332647</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29998782">Fluorescence of Deep Infiltrating Endometriosis During Laparoscopic Surgery: A Preliminary Report on 6 Cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">De Neef A,
|
||
Cadière GB,
|
||
Bourgeois P,
|
||
Barbieux R,
|
||
Dapri G,
|
||
Fastrez M</span><br />
|
||
<span class="medgenPMjournal">Surg Innov</span>
|
||
2018 Oct;25(5):450-454.
|
||
Epub 2018 Jul 12
|
||
doi: 10.1177/1553350618785486.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29998782" target="_blank">29998782</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/18462243">Current considerations in the management of rectovaginal fistula from Crohn's disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hannaway CD,
|
||
Hull TL</span><br />
|
||
<span class="medgenPMjournal">Colorectal Dis</span>
|
||
2008 Oct;10(8):747-55; discussion 755-6.
|
||
Epub 2008 May 4
|
||
doi: 10.1111/j.1463-1318.2008.01552.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18462243" target="_blank">18462243</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11137690">Advances in the management of anorectal malformations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Peña A,
|
||
Hong A</span><br />
|
||
<span class="medgenPMjournal">Am J Surg</span>
|
||
2000 Nov;180(5):370-6.
|
||
doi: 10.1016/s0002-9610(00)00491-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11137690" target="_blank">11137690</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Rectovaginal%20fistula%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 (249)</a></div></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/36735766">Gracilis Muscle Interposition for the Treatment of Rectovaginal Fistula: A Systematic Review and Pooled Analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Maspero M,
|
||
Otero Piñeiro A,
|
||
Steele SR,
|
||
Hull TL</span><br />
|
||
<span class="medgenPMjournal">Dis Colon Rectum</span>
|
||
2023 May 1;66(5):631-645.
|
||
Epub 2023 Feb 3
|
||
doi: 10.1097/DCR.0000000000002739.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36735766" target="_blank">36735766</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32841755">Surgical Outcomes after Colorectal Surgery for Endometriosis: A Systematic Review and Meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bendifallah S,
|
||
Puchar A,
|
||
Vesale E,
|
||
Moawad G,
|
||
Daraï E,
|
||
Roman H</span><br />
|
||
<span class="medgenPMjournal">J Minim Invasive Gynecol</span>
|
||
2021 Mar;28(3):453-466.
|
||
Epub 2020 Aug 22
|
||
doi: 10.1016/j.jmig.2020.08.015.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32841755" target="_blank">32841755</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25284745">Gracilis muscle interposition for rectovaginal and anovaginal fistula repair: a systematic literature review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hotouras A,
|
||
Ribas Y,
|
||
Zakeri S,
|
||
Murphy J,
|
||
Bhan C,
|
||
Chan CL</span><br />
|
||
<span class="medgenPMjournal">Colorectal Dis</span>
|
||
2015 Feb;17(2):104-10.
|
||
doi: 10.1111/codi.12791.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25284745" target="_blank">25284745</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25038961">Gracilis muscle transposition for complex perineal fistulas and sinuses: a systematic literature review of surgical outcomes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Takano S,
|
||
Boutros M,
|
||
Wexner SD</span><br />
|
||
<span class="medgenPMjournal">J Am Coll Surg</span>
|
||
2014 Aug;219(2):313-23.
|
||
Epub 2014 May 2
|
||
doi: 10.1016/j.jamcollsurg.2014.04.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25038961" target="_blank">25038961</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23255878">German S3-Guideline: rectovaginal fistula.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ommer A,
|
||
Herold A,
|
||
Berg E,
|
||
Fürst A,
|
||
Schiedeck T,
|
||
Sailer M</span><br />
|
||
<span class="medgenPMjournal">Ger Med Sci</span>
|
||
2012;10:Doc15.
|
||
Epub 2012 Oct 29
|
||
doi: 10.3205/000166.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23255878" target="_blank">23255878</a><a href="/pmc/articles/PMC3525883" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Rectovaginal%20fistula%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (24)</a></div></div>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C0034895%5bDISCUI%5d&filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (1)</a></li>
|
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<li><a href="/gtr/tests?term=C0034895%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (1)</a></li>
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<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C0034895%5bDISCUI%5d" target="_blank">See all (1)</a></total></li>
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