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Syndrome de Meckel Gruber: à propos d’un cas rare

Meckel Gruber syndrome is a rare autosomal recessive polymalformation syndrome characterized by occipital encephalocele, polydactyly and cystic renal dysplasia. Ultrasound is, at present, the best tool for prenatal screening of this lethal polymalformation and diagnosys is confirmed by karyotyping....

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Dades bibliogràfiques
Publicat a:Pan Afr Med J
Autors principals: Itchimouh, Sanaa, Khabtou, Karima, Mahdaoui, Sakher, Boufettal, Houssine, Samouh, Naima
Format: Artigo
Idioma:Inglês
Publicat: The African Field Epidemiology Network 2016
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5268799/
https://ncbi.nlm.nih.gov/pubmed/28154732
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2016.25.43.9696
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