Published June 17, 2021
| Version v1
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SYNDROME DE MECKEL GRUBER: A PROPOS DUN CAS RARE
Creators
- 1. Resident, Service de maternite,Hopital Mere-Enfant Abderrahim Harouchi, centre hospitalier universitaireIBN ROCHD,faculte de medecine et de pharmacie ,Universite Hassan 2 Casablanca.
- 2. Professeur assistant, Service de maternite,Hopital Mere-Enfant Abderrahim Harouchi, centre hospitalier universitaireIBN ROCHD,faculte de medecine et de pharmacie ,Universite Hassan 2 Casablanca.
- 3. Professeur agrege, Service de maternite,Hopital Mere-Enfant Abderrahim Harouchi, centre hospitalier universitaireIBN ROCHD,faculte de medecine et de pharmacie ,Universite Hassan 2 Casablanca.
- 4. 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.
Description
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.
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