Meckel Gruber Syndrome--a case report.
Indian J Pathol Microbiol
;
2004 Jul; 47(3): 430-2
Article
in English
| 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.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Autopsy
/
Syndrome
/
Female
/
Humans
/
Pregnancy
/
Ultrasonography, Prenatal
/
Adult
Type of study:
Diagnostic study
/
Prognostic study
Language:
English
Journal:
Indian J Pathol Microbiol
Year:
2004
Type:
Article
Similar
MEDLINE
...
LILACS
LIS