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Clinical characteristics of neonates With VACTERL association
Background: The VACTERL association (VA) is the non‐random co‐occurrence of vertebral anomalies, anal atresia, cardiovascular malformations, tracheoesophageal fistula and/or esophageal atresia, renal anomalies, and/or limb anomalies, and is referred to by the first letters of its components. Studie...
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Published in: | Pediatrics international 2012-06, Vol.54 (3), p.361-364 |
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container_title | Pediatrics international |
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creator | Oral, Akgun Caner, Ibrahim Yigiter, Murat Kantarci, Mecit Olgun, Hasim Ceviz, Naci Salman, Ahmet Bedii |
description | Background: The VACTERL association (VA) is the non‐random co‐occurrence of vertebral anomalies, anal atresia, cardiovascular malformations, tracheoesophageal fistula and/or esophageal atresia, renal anomalies, and/or limb anomalies, and is referred to by the first letters of its components. Studies investigating the clinical characteristics of VA patients and probing of the observed current six component types are limited, and none of them is focused on neonates. We investigated the clinical characteristics of our patients diagnosed as having VA in the newborn period.
Methods: We retrospectively reviewed the neonates whose final diagnosis was VACTERL association. Presence of at least three components of previously reported six anomalies was accepted as VACTERL association. Sex, birthweight, gestational age, postnatal age, anomalies of the systems that are included in VA, and the other features were recorded.
Results: There was a male predominance (14/11) of 28 patients; and there were three patients with ambiguous genitalia. The most common observed VACTERL component was vertebral anomalies (n= 26), followed by anal atresia (n= 19), tracheoesophageal fistula/esophageal atresia (n= 17), renal anomalies (n= 15), limb anomalies (n= 15) and cardiac anomalies (n= 14). The most frequent combination was VCTL (n= 4). Fifteen (57%) patients had non‐VACTERL anomalies and the most frequent of these was ambiguous genitalia (n= 3).
Conclusion: VA patients may have different clinical characteristics in different populations, and clinicians may miss some component features if the patients are evaluated after the neonatal period. |
doi_str_mv | 10.1111/j.1442-200X.2012.03566.x |
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Methods: We retrospectively reviewed the neonates whose final diagnosis was VACTERL association. Presence of at least three components of previously reported six anomalies was accepted as VACTERL association. Sex, birthweight, gestational age, postnatal age, anomalies of the systems that are included in VA, and the other features were recorded.
Results: There was a male predominance (14/11) of 28 patients; and there were three patients with ambiguous genitalia. The most common observed VACTERL component was vertebral anomalies (n= 26), followed by anal atresia (n= 19), tracheoesophageal fistula/esophageal atresia (n= 17), renal anomalies (n= 15), limb anomalies (n= 15) and cardiac anomalies (n= 14). The most frequent combination was VCTL (n= 4). Fifteen (57%) patients had non‐VACTERL anomalies and the most frequent of these was ambiguous genitalia (n= 3).
Conclusion: VA patients may have different clinical characteristics in different populations, and clinicians may miss some component features if the patients are evaluated after the neonatal period.</description><identifier>ISSN: 1328-8067</identifier><identifier>EISSN: 1442-200X</identifier><identifier>DOI: 10.1111/j.1442-200X.2012.03566.x</identifier><identifier>PMID: 22300427</identifier><language>eng</language><publisher>Melbourne, Australia: Blackwell Publishing Asia</publisher><subject>Anal Canal - abnormalities ; Birth defects ; Esophagus - abnormalities ; Female ; Heart Defects, Congenital - diagnosis ; Humans ; Infant, Newborn ; Kidney - abnormalities ; Limb Deformities, Congenital - diagnosis ; Male ; neonate ; Newborn babies ; Pediatrics ; Retrospective Studies ; Spine - abnormalities ; Trachea - abnormalities ; VACTERL ; VATER</subject><ispartof>Pediatrics international, 2012-06, Vol.54 (3), p.361-364</ispartof><rights>2012 The Authors. Pediatrics International © 2012 Japan Pediatric Society</rights><rights>2012 The Authors. Pediatrics International © 2012 Japan Pediatric Society.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4596-dd005ad0b05958361c9f635861c1c9d150bfbfb143c212d7b077e503e86a320e3</citedby><cites>FETCH-LOGICAL-c4596-dd005ad0b05958361c9f635861c1c9d150bfbfb143c212d7b077e503e86a320e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22300427$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oral, Akgun</creatorcontrib><creatorcontrib>Caner, Ibrahim</creatorcontrib><creatorcontrib>Yigiter, Murat</creatorcontrib><creatorcontrib>Kantarci, Mecit</creatorcontrib><creatorcontrib>Olgun, Hasim</creatorcontrib><creatorcontrib>Ceviz, Naci</creatorcontrib><creatorcontrib>Salman, Ahmet Bedii</creatorcontrib><title>Clinical characteristics of neonates With VACTERL association</title><title>Pediatrics international</title><addtitle>Pediatr Int</addtitle><description>Background: The VACTERL association (VA) is the non‐random co‐occurrence of vertebral anomalies, anal atresia, cardiovascular malformations, tracheoesophageal fistula and/or esophageal atresia, renal anomalies, and/or limb anomalies, and is referred to by the first letters of its components. Studies investigating the clinical characteristics of VA patients and probing of the observed current six component types are limited, and none of them is focused on neonates. We investigated the clinical characteristics of our patients diagnosed as having VA in the newborn period.
Methods: We retrospectively reviewed the neonates whose final diagnosis was VACTERL association. Presence of at least three components of previously reported six anomalies was accepted as VACTERL association. Sex, birthweight, gestational age, postnatal age, anomalies of the systems that are included in VA, and the other features were recorded.
Results: There was a male predominance (14/11) of 28 patients; and there were three patients with ambiguous genitalia. The most common observed VACTERL component was vertebral anomalies (n= 26), followed by anal atresia (n= 19), tracheoesophageal fistula/esophageal atresia (n= 17), renal anomalies (n= 15), limb anomalies (n= 15) and cardiac anomalies (n= 14). The most frequent combination was VCTL (n= 4). Fifteen (57%) patients had non‐VACTERL anomalies and the most frequent of these was ambiguous genitalia (n= 3).
Conclusion: VA patients may have different clinical characteristics in different populations, and clinicians may miss some component features if the patients are evaluated after the neonatal period.</description><subject>Anal Canal - abnormalities</subject><subject>Birth defects</subject><subject>Esophagus - abnormalities</subject><subject>Female</subject><subject>Heart Defects, Congenital - diagnosis</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Kidney - abnormalities</subject><subject>Limb Deformities, Congenital - diagnosis</subject><subject>Male</subject><subject>neonate</subject><subject>Newborn babies</subject><subject>Pediatrics</subject><subject>Retrospective Studies</subject><subject>Spine - abnormalities</subject><subject>Trachea - abnormalities</subject><subject>VACTERL</subject><subject>VATER</subject><issn>1328-8067</issn><issn>1442-200X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqNkUlPwzAQhS0EYv8LKBIXLgljO1564IBKWURZhKBws1zHES5pUuxUlH-PQ6EHTngOfpK_Nx69QSjBkOF4jicZznOSEoCXjAAmGVDGebZYQ9urh_WoKZGpBC620E4IEwCQQuabaIsQCpATsY1O-pWrndFVYl6116a13oXWmZA0ZVLbptatDcmza1-T0Wn_cfAwTHQIjXG6dU29hzZKXQW7_3PvoqfzwWP_Mh3eXVz1T4epyVmPp0UBwHQBY2A9JinHpldyymQUURaYwbiMhXNqCCaFGIMQlgG1kmtKwNJddLTsO_PN-9yGVk1dMLaqdBxxHhQGLDjBjOYRPfyDTpq5r-N0HcU5F7mQkZJLyvgmBG9LNfNuqv1nhFQXsZqoLknVJam6iNV3xGoRrQc_H8zHU1usjL-ZRuBkCXy4yn7-u7G6H5x1KvrTpT8uwi5Wfu3fFBdUMPV8e6FGDy83cDu6VpJ-AdNIluo</recordid><startdate>201206</startdate><enddate>201206</enddate><creator>Oral, Akgun</creator><creator>Caner, Ibrahim</creator><creator>Yigiter, Murat</creator><creator>Kantarci, Mecit</creator><creator>Olgun, Hasim</creator><creator>Ceviz, Naci</creator><creator>Salman, Ahmet Bedii</creator><general>Blackwell Publishing Asia</general><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201206</creationdate><title>Clinical characteristics of neonates With VACTERL association</title><author>Oral, Akgun ; Caner, Ibrahim ; Yigiter, Murat ; Kantarci, Mecit ; Olgun, Hasim ; Ceviz, Naci ; Salman, Ahmet Bedii</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4596-dd005ad0b05958361c9f635861c1c9d150bfbfb143c212d7b077e503e86a320e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Anal Canal - abnormalities</topic><topic>Birth defects</topic><topic>Esophagus - abnormalities</topic><topic>Female</topic><topic>Heart Defects, Congenital - diagnosis</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Kidney - abnormalities</topic><topic>Limb Deformities, Congenital - diagnosis</topic><topic>Male</topic><topic>neonate</topic><topic>Newborn babies</topic><topic>Pediatrics</topic><topic>Retrospective Studies</topic><topic>Spine - abnormalities</topic><topic>Trachea - abnormalities</topic><topic>VACTERL</topic><topic>VATER</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oral, Akgun</creatorcontrib><creatorcontrib>Caner, Ibrahim</creatorcontrib><creatorcontrib>Yigiter, Murat</creatorcontrib><creatorcontrib>Kantarci, Mecit</creatorcontrib><creatorcontrib>Olgun, Hasim</creatorcontrib><creatorcontrib>Ceviz, Naci</creatorcontrib><creatorcontrib>Salman, Ahmet Bedii</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatrics international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oral, Akgun</au><au>Caner, Ibrahim</au><au>Yigiter, Murat</au><au>Kantarci, Mecit</au><au>Olgun, Hasim</au><au>Ceviz, Naci</au><au>Salman, Ahmet Bedii</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical characteristics of neonates With VACTERL association</atitle><jtitle>Pediatrics international</jtitle><addtitle>Pediatr Int</addtitle><date>2012-06</date><risdate>2012</risdate><volume>54</volume><issue>3</issue><spage>361</spage><epage>364</epage><pages>361-364</pages><issn>1328-8067</issn><eissn>1442-200X</eissn><abstract>Background: The VACTERL association (VA) is the non‐random co‐occurrence of vertebral anomalies, anal atresia, cardiovascular malformations, tracheoesophageal fistula and/or esophageal atresia, renal anomalies, and/or limb anomalies, and is referred to by the first letters of its components. Studies investigating the clinical characteristics of VA patients and probing of the observed current six component types are limited, and none of them is focused on neonates. We investigated the clinical characteristics of our patients diagnosed as having VA in the newborn period.
Methods: We retrospectively reviewed the neonates whose final diagnosis was VACTERL association. Presence of at least three components of previously reported six anomalies was accepted as VACTERL association. Sex, birthweight, gestational age, postnatal age, anomalies of the systems that are included in VA, and the other features were recorded.
Results: There was a male predominance (14/11) of 28 patients; and there were three patients with ambiguous genitalia. The most common observed VACTERL component was vertebral anomalies (n= 26), followed by anal atresia (n= 19), tracheoesophageal fistula/esophageal atresia (n= 17), renal anomalies (n= 15), limb anomalies (n= 15) and cardiac anomalies (n= 14). The most frequent combination was VCTL (n= 4). Fifteen (57%) patients had non‐VACTERL anomalies and the most frequent of these was ambiguous genitalia (n= 3).
Conclusion: VA patients may have different clinical characteristics in different populations, and clinicians may miss some component features if the patients are evaluated after the neonatal period.</abstract><cop>Melbourne, Australia</cop><pub>Blackwell Publishing Asia</pub><pmid>22300427</pmid><doi>10.1111/j.1442-200X.2012.03566.x</doi><tpages>4</tpages></addata></record> |
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subjects | Anal Canal - abnormalities Birth defects Esophagus - abnormalities Female Heart Defects, Congenital - diagnosis Humans Infant, Newborn Kidney - abnormalities Limb Deformities, Congenital - diagnosis Male neonate Newborn babies Pediatrics Retrospective Studies Spine - abnormalities Trachea - abnormalities VACTERL VATER |
title | Clinical characteristics of neonates With VACTERL association |
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