VACTERL Associated with a Rare Limb Anomaly Combined with Edward (Trisomy 18) Syndrome

VACTERL association is a heterogeneous condition that includes at least three out of six core structural defects which occur together more commonly than would be expected by chance alone. We report a rare association of VACTERL with unilateral proximal focal femoral deficiency and trisomy 18 syndrom...

Descripción completa

Detalles Bibliográficos
Autores principales: Hasan, Zaheer, Thakur, Vinit Kumar, Chaubey, Digamber, Rahul, Sandip Kumar, Kumar, Sujit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Images
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286019/
https://www.ncbi.nlm.nih.gov/pubmed/34321798
http://dx.doi.org/10.4103/jiaps.JIAPS_237_20
_version_ 1783723656964210688
author Hasan, Zaheer
Thakur, Vinit Kumar
Chaubey, Digamber
Rahul, Sandip Kumar
Kumar, Sujit
author_facet Hasan, Zaheer
Thakur, Vinit Kumar
Chaubey, Digamber
Rahul, Sandip Kumar
Kumar, Sujit
author_sort Hasan, Zaheer
collection PubMed
description VACTERL association is a heterogeneous condition that includes at least three out of six core structural defects which occur together more commonly than would be expected by chance alone. We report a rare association of VACTERL with unilateral proximal focal femoral deficiency and trisomy 18 syndrome.
format Online
Article
Text
id pubmed-8286019
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Wolters Kluwer - Medknow
record_format MEDLINE/PubMed
spelling pubmed-82860192021-07-27 VACTERL Associated with a Rare Limb Anomaly Combined with Edward (Trisomy 18) Syndrome Hasan, Zaheer Thakur, Vinit Kumar Chaubey, Digamber Rahul, Sandip Kumar Kumar, Sujit J Indian Assoc Pediatr Surg Images VACTERL association is a heterogeneous condition that includes at least three out of six core structural defects which occur together more commonly than would be expected by chance alone. We report a rare association of VACTERL with unilateral proximal focal femoral deficiency and trisomy 18 syndrome. Wolters Kluwer - Medknow 2021 2021-05-17 /pmc/articles/PMC8286019/ /pubmed/34321798 http://dx.doi.org/10.4103/jiaps.JIAPS_237_20 Text en Copyright: © 2021 Journal of Indian Association of Pediatric Surgeons https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Images
Hasan, Zaheer
Thakur, Vinit Kumar
Chaubey, Digamber
Rahul, Sandip Kumar
Kumar, Sujit
VACTERL Associated with a Rare Limb Anomaly Combined with Edward (Trisomy 18) Syndrome
title VACTERL Associated with a Rare Limb Anomaly Combined with Edward (Trisomy 18) Syndrome
title_full VACTERL Associated with a Rare Limb Anomaly Combined with Edward (Trisomy 18) Syndrome
title_fullStr VACTERL Associated with a Rare Limb Anomaly Combined with Edward (Trisomy 18) Syndrome
title_full_unstemmed VACTERL Associated with a Rare Limb Anomaly Combined with Edward (Trisomy 18) Syndrome
title_short VACTERL Associated with a Rare Limb Anomaly Combined with Edward (Trisomy 18) Syndrome
title_sort vacterl associated with a rare limb anomaly combined with edward (trisomy 18) syndrome
topic Images
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286019/
https://www.ncbi.nlm.nih.gov/pubmed/34321798
http://dx.doi.org/10.4103/jiaps.JIAPS_237_20
work_keys_str_mv AT hasanzaheer vacterlassociatedwithararelimbanomalycombinedwithedwardtrisomy18syndrome
AT thakurvinitkumar vacterlassociatedwithararelimbanomalycombinedwithedwardtrisomy18syndrome
AT chaubeydigamber vacterlassociatedwithararelimbanomalycombinedwithedwardtrisomy18syndrome
AT rahulsandipkumar vacterlassociatedwithararelimbanomalycombinedwithedwardtrisomy18syndrome
AT kumarsujit vacterlassociatedwithararelimbanomalycombinedwithedwardtrisomy18syndrome

Ejemplares similares