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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Bibliografiske detaljer
Udgivet i:Pan Afr Med J
Main Authors: Itchimouh, Sanaa, Khabtou, Karima, Mahdaoui, Sakher, Boufettal, Houssine, Samouh, Naima
Format: Artigo
Sprog:Inglês
Udgivet: The African Field Epidemiology Network 2016
Fag:
Case Report
Online adgang: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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