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  • Title: Fetal autopsy of Meckel Gruber syndrome -a case report.
    Author: Bolineni C, Nagamuthu EA, Neelala N.
    Journal: Fetal Pediatr Pathol; 2013 Oct; 32(5):387-93. PubMed ID: 23445452.
    Abstract:
    Meckel Gruber syndrome is a rare autosomal recessive lethal malformation characterized by typical manifestations of occipital encephalocele, bilateral polycystic kidneys and post-axial polydactyly. One such rare case at 28 weeks of gestation was terminated and its case report with the phenotypic features, fetal autopsy and histo-pathological examination are discussed.
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