[Meckel Gruber syndrome: about a rare case]. / Syndrome de Meckel Gruber: à propos d'un cas rare.
Pan Afr Med J
; 25: 43, 2016.
Article
en Fr
| MEDLINE
| ID: mdl-28154732
ABSTRACT
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. We here report a case of Meckel Gruber syndrome detected by ultrasound. Abortion was performed at 25 weeks of amenorrhoea.
Palabras clave
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Ultrasonografía Prenatal
/
Trastornos de la Motilidad Ciliar
/
Aborto Inducido
/
Encefalocele
/
Enfermedades Renales Poliquísticas
Tipo de estudio:
Diagnostic_studies
Límite:
Adult
/
Female
/
Humans
/
Pregnancy
Idioma:
Fr
Revista:
Pan Afr Med J
Año:
2016
Tipo del documento:
Article
País de afiliación:
Marruecos