Meckel Gruber Syndrome--a case report.
Indian J Pathol Microbiol
;
2004 Jul; 47(3): 430-2
Artículo
en Inglés
| 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.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Autopsia
/
Síndrome
/
Femenino
/
Humanos
/
Embarazo
/
Ultrasonografía Prenatal
/
Adulto
Tipo de estudio:
Estudio diagnóstico
/
Estudio pronóstico
Idioma:
Inglés
Revista:
Indian J Pathol Microbiol
Año:
2004
Tipo del documento:
Artículo
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