Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Pediatrics international 2012-06, Vol.54 (3), p.361-364
Main Authors: Oral, Akgun, Caner, Ibrahim, Yigiter, Murat, Kantarci, Mecit, Olgun, Hasim, Ceviz, Naci, Salman, Ahmet Bedii
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c4596-dd005ad0b05958361c9f635861c1c9d150bfbfb143c212d7b077e503e86a320e3
cites cdi_FETCH-LOGICAL-c4596-dd005ad0b05958361c9f635861c1c9d150bfbfb143c212d7b077e503e86a320e3
container_end_page 364
container_issue 3
container_start_page 361
container_title Pediatrics international
container_volume 54
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1017621534</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1017621534</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4596-dd005ad0b05958361c9f635861c1c9d150bfbfb143c212d7b077e503e86a320e3</originalsourceid><addsrcrecordid>eNqNkUlPwzAQhS0EYv8LKBIXLgljO1564IBKWURZhKBws1zHES5pUuxUlH-PQ6EHTngOfpK_Nx69QSjBkOF4jicZznOSEoCXjAAmGVDGebZYQ9urh_WoKZGpBC620E4IEwCQQuabaIsQCpATsY1O-pWrndFVYl6116a13oXWmZA0ZVLbptatDcmza1-T0Wn_cfAwTHQIjXG6dU29hzZKXQW7_3PvoqfzwWP_Mh3eXVz1T4epyVmPp0UBwHQBY2A9JinHpldyymQUURaYwbiMhXNqCCaFGIMQlgG1kmtKwNJddLTsO_PN-9yGVk1dMLaqdBxxHhQGLDjBjOYRPfyDTpq5r-N0HcU5F7mQkZJLyvgmBG9LNfNuqv1nhFQXsZqoLknVJam6iNV3xGoRrQc_H8zHU1usjL-ZRuBkCXy4yn7-u7G6H5x1KvrTpT8uwi5Wfu3fFBdUMPV8e6FGDy83cDu6VpJ-AdNIluo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1016667478</pqid></control><display><type>article</type><title>Clinical characteristics of neonates With VACTERL association</title><source>Wiley</source><creator>Oral, Akgun ; Caner, Ibrahim ; Yigiter, Murat ; Kantarci, Mecit ; Olgun, Hasim ; Ceviz, Naci ; Salman, Ahmet Bedii</creator><creatorcontrib>Oral, Akgun ; Caner, Ibrahim ; Yigiter, Murat ; Kantarci, Mecit ; Olgun, Hasim ; Ceviz, Naci ; Salman, Ahmet Bedii</creatorcontrib><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><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 &amp; 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>
fulltext fulltext
identifier ISSN: 1328-8067
ispartof Pediatrics international, 2012-06, Vol.54 (3), p.361-364
issn 1328-8067
1442-200X
language eng
recordid cdi_proquest_miscellaneous_1017621534
source Wiley
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T03%3A10%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Clinical%20characteristics%20of%20neonates%20With%20VACTERL%20association&rft.jtitle=Pediatrics%20international&rft.au=Oral,%20Akgun&rft.date=2012-06&rft.volume=54&rft.issue=3&rft.spage=361&rft.epage=364&rft.pages=361-364&rft.issn=1328-8067&rft.eissn=1442-200X&rft_id=info:doi/10.1111/j.1442-200X.2012.03566.x&rft_dat=%3Cproquest_cross%3E1017621534%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4596-dd005ad0b05958361c9f635861c1c9d150bfbfb143c212d7b077e503e86a320e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1016667478&rft_id=info:pmid/22300427&rfr_iscdi=true