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VACTERL association-type anomalies in a male neonate with a Y-chromosome abnormality

The acronym VACTERL describes the non-random co-occurrence of three of the following anomalies: vertebral (V), anal (A), cardiac (C), tracheoesophageal fistula with or without oesophageal atresia (TE), renal (R) and limb defects (L). Here, we report a newborn baby with VACTERL-type anomalies along w...

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Autor principal: Bhagat, Manish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369973/
https://www.ncbi.nlm.nih.gov/pubmed/25988067
http://dx.doi.org/10.1093/omcr/omu062
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author Bhagat, Manish
author_facet Bhagat, Manish
author_sort Bhagat, Manish
collection PubMed
description The acronym VACTERL describes the non-random co-occurrence of three of the following anomalies: vertebral (V), anal (A), cardiac (C), tracheoesophageal fistula with or without oesophageal atresia (TE), renal (R) and limb defects (L). Here, we report a newborn baby with VACTERL-type anomalies along with a single umbilical artery. The additional interesting findings include development dysplasia of the right hip, dislocation of the left knee and the left club foot. The karyotype revealed 46, X,i (Yp), i.e. deletion in the long arm, while duplication in the short arm of the Y chromosome (isochromosome Yp), which has never been previously reported in VACTERL association.
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spelling pubmed-43699732015-05-18 VACTERL association-type anomalies in a male neonate with a Y-chromosome abnormality Bhagat, Manish Oxf Med Case Reports Case Reports The acronym VACTERL describes the non-random co-occurrence of three of the following anomalies: vertebral (V), anal (A), cardiac (C), tracheoesophageal fistula with or without oesophageal atresia (TE), renal (R) and limb defects (L). Here, we report a newborn baby with VACTERL-type anomalies along with a single umbilical artery. The additional interesting findings include development dysplasia of the right hip, dislocation of the left knee and the left club foot. The karyotype revealed 46, X,i (Yp), i.e. deletion in the long arm, while duplication in the short arm of the Y chromosome (isochromosome Yp), which has never been previously reported in VACTERL association. Oxford University Press 2015-01-10 /pmc/articles/PMC4369973/ /pubmed/25988067 http://dx.doi.org/10.1093/omcr/omu062 Text en © The Author 2015. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Reports
Bhagat, Manish
VACTERL association-type anomalies in a male neonate with a Y-chromosome abnormality
title VACTERL association-type anomalies in a male neonate with a Y-chromosome abnormality
title_full VACTERL association-type anomalies in a male neonate with a Y-chromosome abnormality
title_fullStr VACTERL association-type anomalies in a male neonate with a Y-chromosome abnormality
title_full_unstemmed VACTERL association-type anomalies in a male neonate with a Y-chromosome abnormality
title_short VACTERL association-type anomalies in a male neonate with a Y-chromosome abnormality
title_sort vacterl association-type anomalies in a male neonate with a y-chromosome abnormality
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369973/
https://www.ncbi.nlm.nih.gov/pubmed/25988067
http://dx.doi.org/10.1093/omcr/omu062
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