Meckel Gruber Syndrome is a rare and lethal autosomal recessive congenital anomaly syndrome, characterized by triad of : occipital encephalocele Postaxial polydactyly, bilateral dysplastic cystic kidneys other occasional features. Diagnosis can be made on ultrasonography with atleast two the major Here we present pregnant women complicated meckel gruber syndrome. We relayed findings MRI ,pregan...

Meckel-Gruber syndrome is a rare autosomal recessive lethal malformation characterized by typical manifestations of occipital encephalocele, bilateral polycystic kidneys and post axial polydactyly. The worldwide incidence varies from 1 in 13,250 to 1 in 140,000 live births. Highest incidence was reported in Gujarati Indians. We report a rare case of Meckel-Gruber syndrome and review of literature.

El onfalocele o exónfalos se definen como un defecto congénito de la pared abdominal, que consiste en herniación las vísceras abdominales a través del anillo umbilical. Esta entidad rara vez asocia comunicación divertículo Meckel con el saco onfalocele. Teniendo cuenta escasa prevalencia dicha entidad, compartimos reporte caso paciente recién nacido, diagnóstico menor, quien sospechaba ruptura ...

Meckel Gruber syndrome was originally described by Meckel in 1822, later by Gruber and more recently by Opitz and Howe.1 It is a lethal autosomal recessive disorder characterized by the triad of encephalocele, polycystic kidneys and polydactyly. Prenatal ultrasonographic diagnosis of this condition has been reported extensively during the second and third trimeter. In the low risk population th...

Meckel diverticulum (MD) is one of the most common congenital gastrointestinal anomalies and occurs in 1.2-2% of the general population. MD usually presents with massive painless rectal bleeding, intestinal obstruction or inflammation in children and adults. Suppurative Meckel diverticulitis is uncommon in children. An experience is described of a 3-year-old girl with suppurative inflammation i...

Le diverticule de Meckel est une affection rare qui touche 2% de la population générale. Le plus souvent asymptomatique, le diverticule de Meckel peut se manifester par des douleurs de la fosse iliaque droite mais il peut aussi se révéler parfois chez l'enfant ou l'adulte jeune par des complications : occlusion, infection dite diverticulite, hémorragie digestive basse.la perforation est le plus...

Abstract Le syndrome de Meckel Gruber est un syndrome poly malformatif rare, de transmission autosomique récessive, défini par d'encéphalocèle occipital, polydactylie et dysplasie kystique rénale. L'échographie constitue, à l'heure actuelle, le meilleur moyen de dépistage anténatal de cette poly malformation létale et sa confirmation se fait par l'étude du caryotype. Nous rapportons un cas de s...