Mowat-Wilson syndrome in a Moroccan consanguineous family

Mowat-Wilson syndrome is a mental retardation-multiple congenital anomaly syndrome characterized by a typical facies, developmental delay, epilepsy, and variable congenital malformations, including Hirschsprung disease, urogenital anomalies, congenital heart disease, and agenesis of the corpus callo...

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Detalles Bibliográficos
Autores principales: Ratbi, Ilham, Elalaoui, Chafai Siham, Dastot-Le, Moal Florence, Goossens, Michel, Giurgea, Irina, Sefiani, Abdelaziz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2007
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168139/
https://www.ncbi.nlm.nih.gov/pubmed/21957361
http://dx.doi.org/10.4103/0971-6866.38988

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168139/
https://www.ncbi.nlm.nih.gov/pubmed/21957361
http://dx.doi.org/10.4103/0971-6866.38988

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