Preaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa

Trisomy 13 is a chromosomal disorder characterized by a severe clinical picture of multiple congenital anomalies. We here describe the clinical and genetic features and prognosis observed in a newborn with trisomy 13 from Central Africa. He presented the rare feature of preaxial polydactyly of the f...

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Autores principales: Mbuyi-Musanzayi, Sébastien, Lumaka, Aimé, Yogolelo Asani, Bienvenu, Lubala Kasole, Toni, Lukusa Tshilobo, Prosper, Kalenga Muenze, Prosper, Tshilombo Katombe, François, Devriendt, Koenraad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164427/
https://www.ncbi.nlm.nih.gov/pubmed/25254124
http://dx.doi.org/10.1155/2014/365031
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author Mbuyi-Musanzayi, Sébastien
Lumaka, Aimé
Yogolelo Asani, Bienvenu
Lubala Kasole, Toni
Lukusa Tshilobo, Prosper
Kalenga Muenze, Prosper
Tshilombo Katombe, François
Devriendt, Koenraad
author_facet Mbuyi-Musanzayi, Sébastien
Lumaka, Aimé
Yogolelo Asani, Bienvenu
Lubala Kasole, Toni
Lukusa Tshilobo, Prosper
Kalenga Muenze, Prosper
Tshilombo Katombe, François
Devriendt, Koenraad
author_sort Mbuyi-Musanzayi, Sébastien
collection PubMed
description Trisomy 13 is a chromosomal disorder characterized by a severe clinical picture of multiple congenital anomalies. We here describe the clinical and genetic features and prognosis observed in a newborn with trisomy 13 from Central Africa. He presented the rare feature of preaxial polydactyly of the feet.
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spelling pubmed-41644272014-09-24 Preaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa Mbuyi-Musanzayi, Sébastien Lumaka, Aimé Yogolelo Asani, Bienvenu Lubala Kasole, Toni Lukusa Tshilobo, Prosper Kalenga Muenze, Prosper Tshilombo Katombe, François Devriendt, Koenraad Case Rep Genet Case Report Trisomy 13 is a chromosomal disorder characterized by a severe clinical picture of multiple congenital anomalies. We here describe the clinical and genetic features and prognosis observed in a newborn with trisomy 13 from Central Africa. He presented the rare feature of preaxial polydactyly of the feet. Hindawi Publishing Corporation 2014 2014-09-01 /pmc/articles/PMC4164427/ /pubmed/25254124 http://dx.doi.org/10.1155/2014/365031 Text en Copyright © 2014 Sébastien Mbuyi-Musanzayi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Mbuyi-Musanzayi, Sébastien
Lumaka, Aimé
Yogolelo Asani, Bienvenu
Lubala Kasole, Toni
Lukusa Tshilobo, Prosper
Kalenga Muenze, Prosper
Tshilombo Katombe, François
Devriendt, Koenraad
Preaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa
title Preaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa
title_full Preaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa
title_fullStr Preaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa
title_full_unstemmed Preaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa
title_short Preaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa
title_sort preaxial polydactyly of the foot: variable expression of trisomy 13 in a case from central africa
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164427/
https://www.ncbi.nlm.nih.gov/pubmed/25254124
http://dx.doi.org/10.1155/2014/365031
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