SYNDROME DE MECKEL GRUBER: A PROPOS DUN CAS RARE
- Resident, Service de maternite,Hopital Mere-Enfant Abderrahim Harouchi, centre hospitalier universitaireIBN ROCHD,faculte de medecine et de pharmacie ,Universite Hassan 2 Casablanca.
- Professeur assistant, Service de maternite,Hopital Mere-Enfant Abderrahim Harouchi, centre hospitalier universitaireIBN ROCHD,faculte de medecine et de pharmacie ,Universite Hassan 2 Casablanca.
- Professeur agrege, Service de maternite,Hopital Mere-Enfant Abderrahim Harouchi, centre hospitalier universitaireIBN ROCHD,faculte de medecine et de pharmacie ,Universite Hassan 2 Casablanca.
- Chef de service Service de maternite,Hopital Mere-Enfant Abderrahim Harouchi, centre hospitalier universitaireIBN ROCHD,faculte de medecine et de pharmacie ,Universite Hassan 2 Casablanca.
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Meckel-Gruber syndrome is a monogenic congenital disorder characterized by occipital encephalocele, polydactyly, and polycystic kidneys. This syndrome is incompatible with life. We report a case diagnosed on fetal ultrasound at a gestational age of 22 SA and 6 days, presenting the clinical triad of Meckel-Gruber syndrome. A medical termination of the pregnancy was indicated. From this rare case, and through a review of the literature, we will discuss the different clinical, ultrasound and prognostic aspects of this rare pathology.
[B. Ouafidi, O. Wajih, F. Elmiski, H. Kiram, M. Jalal, A. Lamrissi, K. Fichtali and S. Bouhya (2021); SYNDROME DE MECKEL GRUBER: A PROPOS DUN CAS RARE Int. J. of Adv. Res. 9 (Jun). 365-369] (ISSN 2320-5407). www.journalijar.com
Wajih Oumaima, Fatiha ELmiski,Hamza Kiram, Jalal Mohamed,Lamrissi Amine, Fichtali Karima, Bouhya Said
Morocco
