Literature DB >> 16295449

Meckel Gruber Syndrome--a case report.

S R Desai1, J V Wader.   

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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Year:  2004        PMID: 16295449

Source DB:  PubMed          Journal:  Indian J Pathol Microbiol        ISSN: 0377-4929            Impact factor:   0.740


  2 in total

1.  Meckel-Gruber syndrome: Antenatal diagnosis and ethical perspectives.

Authors:  Sarar Mohamed; Fatima Ibrahim; Kameel Kamil; Satti A Satti
Journal:  Sudan J Paediatr       Date:  2012

2.  [Meckel Gruber syndrome: about a rare case].

Authors:  Sanaa Itchimouh; Karima Khabtou; Sakher Mahdaoui; Houssine Boufettal; Naima Samouh
Journal:  Pan Afr Med J       Date:  2016-09-29
  2 in total

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