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Neonate with VACTERL Association and a Branchial Arch Anomaly without Hydrocephalus

VACTERL (vertebral anomalies, anal atresia, cardiac defect, tracheoesophageal fistula, renal anomaly, limb anomalies) is an association of anomalies with a wide spectrum of phenotypic expression. While the majority of cases are sporadic, there is evidence of an inherited component in a small number...

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Detalles Bibliográficos
Autores principales: Velazquez, Danitza, Pereira, Elaine, Havranek, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Medical Publishers 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737631/
https://www.ncbi.nlm.nih.gov/pubmed/26929876
http://dx.doi.org/10.1055/s-0035-1566297
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author Velazquez, Danitza
Pereira, Elaine
Havranek, Thomas
author_facet Velazquez, Danitza
Pereira, Elaine
Havranek, Thomas
author_sort Velazquez, Danitza
collection PubMed
description VACTERL (vertebral anomalies, anal atresia, cardiac defect, tracheoesophageal fistula, renal anomaly, limb anomalies) is an association of anomalies with a wide spectrum of phenotypic expression. While the majority of cases are sporadic, there is evidence of an inherited component in a small number of patients as well as the potential influence of nongenetic risk factors (maternal diabetes mellitus). Presence of hydrocephalus has been reported in VACTERL patients (VACTERL-H) in the past, with some displaying branchial arch anomalies. We report the unique case of an infant of diabetic mother with VACTERL association and a branchial arch anomaly—in the absence of hydrocephalus.
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spelling pubmed-47376312016-03-01 Neonate with VACTERL Association and a Branchial Arch Anomaly without Hydrocephalus Velazquez, Danitza Pereira, Elaine Havranek, Thomas AJP Rep Article VACTERL (vertebral anomalies, anal atresia, cardiac defect, tracheoesophageal fistula, renal anomaly, limb anomalies) is an association of anomalies with a wide spectrum of phenotypic expression. While the majority of cases are sporadic, there is evidence of an inherited component in a small number of patients as well as the potential influence of nongenetic risk factors (maternal diabetes mellitus). Presence of hydrocephalus has been reported in VACTERL patients (VACTERL-H) in the past, with some displaying branchial arch anomalies. We report the unique case of an infant of diabetic mother with VACTERL association and a branchial arch anomaly—in the absence of hydrocephalus. Thieme Medical Publishers 2015-11-02 2016-03 /pmc/articles/PMC4737631/ /pubmed/26929876 http://dx.doi.org/10.1055/s-0035-1566297 Text en © Thieme Medical Publishers
spellingShingle Article
Velazquez, Danitza
Pereira, Elaine
Havranek, Thomas
Neonate with VACTERL Association and a Branchial Arch Anomaly without Hydrocephalus
title Neonate with VACTERL Association and a Branchial Arch Anomaly without Hydrocephalus
title_full Neonate with VACTERL Association and a Branchial Arch Anomaly without Hydrocephalus
title_fullStr Neonate with VACTERL Association and a Branchial Arch Anomaly without Hydrocephalus
title_full_unstemmed Neonate with VACTERL Association and a Branchial Arch Anomaly without Hydrocephalus
title_short Neonate with VACTERL Association and a Branchial Arch Anomaly without Hydrocephalus
title_sort neonate with vacterl association and a branchial arch anomaly without hydrocephalus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737631/
https://www.ncbi.nlm.nih.gov/pubmed/26929876
http://dx.doi.org/10.1055/s-0035-1566297
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