Cargando…
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...
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: | |
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 |
Ejemplares similares
-
Meningocele in a Congolese Female with Beckwith-Wiedemann Phenotype
por: Mbuyi-Musanzayi, Sébastien, et al.
Publicado: (2014) -
Sacrococcygeal teratoma in a female newborn with clinical features of trisomy 13: a case report from Central Africa
por: Lubala, Toni Kasole, et al.
Publicado: (2015) -
Fragile X checklists: A meta‐analysis and development of a simplified universal clinical checklist
por: Lubala, Toni Kasole, et al.
Publicado: (2018) -
Williams–Beuren syndrome: pitfalls for diagnosis in limited resources setting
por: Lumaka, Aimé, et al.
Publicado: (2016) -
Etude du strabisme chez des enfants de 0 à 15 ans suivis a Lubumbashi, République Démocratique du Congo: analyse des aspects épidémiologiques et cliniques
por: Bienvenu, Yogolelo Asani, et al.
Publicado: (2015)