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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Detalles Bibliográficos
Main Authors: Mbuyi-Musanzayi, Sébastien, Lumaka, Aimé, Yogolelo Asani, Bienvenu, Lubala Kasole, Toni, Lukusa Tshilobo, Prosper, Kalenga Muenze, Prosper, Tshilombo Katombe, François, Devriendt, Koenraad
Formato: Artigo
Idioma:Inglês
Publicado: Hindawi Publishing Corporation 2014
Assuntos:
Case Report
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4164427/
https://ncbi.nlm.nih.gov/pubmed/25254124
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2014/365031
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