Preaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa
Joint Authors
Mbuyi-Musanzayi, Sébastien
Lumaka, Aimé
Yogolelo Asani, Bienvenu
Lubala Kasole, Toni
Lukusa Tshilobo, Prosper
Kalenga Muenze, Prosper
Tshilombo Katombe, François
Devriendt, Koenraad
Source
Issue
Vol. 2014, Issue 2014 (31 Dec. 2014), pp.1-5, 5 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2014-08-31
Country of Publication
Egypt
No. of Pages
5
Main Subjects
Abstract EN
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.
American Psychological Association (APA)
Mbuyi-Musanzayi, Sébastien& Lumaka, Aimé& Yogolelo Asani, Bienvenu& Lubala Kasole, Toni& Lukusa Tshilobo, Prosper& Kalenga Muenze, Prosper…[et al.]. 2014. Preaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa. Case Reports in Genetics،Vol. 2014, no. 2014, pp.1-5.
https://search.emarefa.net/detail/BIM-1017038
Modern Language Association (MLA)
Mbuyi-Musanzayi, Sébastien…[et al.]. Preaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa. Case Reports in Genetics No. 2014 (2014), pp.1-5.
https://search.emarefa.net/detail/BIM-1017038
American Medical Association (AMA)
Mbuyi-Musanzayi, Sébastien& Lumaka, Aimé& Yogolelo Asani, Bienvenu& Lubala Kasole, Toni& Lukusa Tshilobo, Prosper& Kalenga Muenze, Prosper…[et al.]. Preaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa. Case Reports in Genetics. 2014. Vol. 2014, no. 2014, pp.1-5.
https://search.emarefa.net/detail/BIM-1017038
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1017038
