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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2015
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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. |
format | Online Article Text |
id | pubmed-4369973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT bhagatmanish vacterlassociationtypeanomaliesinamaleneonatewithaychromosomeabnormality |