Meckel Gruber Syndrome--a case report.
Indian J Pathol Microbiol
;
2004 Jul; 47(3): 430-2
Article
Dans Anglais
| IMSEAR
| ID: sea-72744
ABSTRACT
Meckel Gruber Syndrome is a rare syndrome inherited as Mendelian autosomal recessive condition. The affected infant usually has a large occipital encephalocoele associated with renal cysts and sometimes polydactyly. The prognosis is poor. The affected child is still born or dies early in infancy. If diagnosis is done by prenatal ultrasound examination termination of pregnancy can be done.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Autopsie
/
Syndrome
/
Femelle
/
Humains
/
Grossesse
/
Échographie prénatale
/
Adulte
Type d'étude:
Etude diagnostique
/
Étude pronostique
langue:
Anglais
Texte intégral:
Indian J Pathol Microbiol
Année:
2004
Type:
Article
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