Meckel Gruber Syndrome--a case report.

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Date
2004-07-22
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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.
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Desai SR, Wader JV. Meckel Gruber Syndrome--a case report. Indian Journal of Pathology & Microbiology. 2004 Jul; 47(3): 430-2
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https://imsear.searo.who.int/handle/123456789/72744
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Indian Journal of Pathology & Microbiology