An International Publisher for Academic and Scientific Journals
Author Login
Scholars Journal of Medical Case Reports | Volume-5 | Issue-12
Meckel Gruber Syndrome-An Autopsy Report of a Rare Case
Nanda Patil, Chetan Khurana, Gayatri Patel
Published: Dec. 30, 2017 |
138
169
DOI: 10.36347/sjmcr.2017.v05i12.014
Pages: 857-860
Downloads
Abstract
Meckel Gruber Syndrome is a rare autosomal recessive disorder characterized by a typical clinical triad of meningo-encephalocele, polycystic kidneys and polydactyly. The worldwide incidence varies from 1 in 13250 to 1 in 140000 live births. Highest incidence was reported in Gujrati Indians. We report autopsy features of a Meckel Gruber Syndrome in a 22 weeks female fetus