Abstract |
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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Authors | Sébastien Mbuyi-Musanzayi, Aimé Lumaka, Bienvenu Yogolelo Asani, Toni Lubala Kasole, Prosper Lukusa Tshilobo, Prosper Kalenga Muenze, François Tshilombo Katombe, Koenraad Devriendt |
Journal | Case reports in genetics
(Case Rep Genet)
Vol. 2014
Pg. 365031
( 2014)
ISSN: 2090-6544 [Print] United States |
PMID | 25254124
(Publication Type: Journal Article)
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