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Meckel-Gruber syndrome: A rare and lethal anomaly with review of literature.
MedLine Citation:
PMID:  24082939     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
Meckel-Gruber syndrome is a rare autosomal recessive lethal malformation characterized by typical manifestations of occipital encephalocele, bilateral polycystic kidneys and post axial polydactyly. The worldwide incidence varies from 1 in 13,250 to 1 in 140,000 live births. Highest incidence was reported in Gujarati Indians. We report a rare case of Meckel-Gruber syndrome and review of literature.
Authors:
Sandesh V Parelkar; Satish P Kapadnis; Beejal V Sanghvi; Prashant B Joshi; Dinesh Mundada; Sanjay N Oak
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Journal of pediatric neurosciences     Volume:  8     ISSN:  1817-1745     ISO Abbreviation:  J Pediatr Neurosci     Publication Date:  2013 May 
Date Detail:
Created Date:  2013-10-01     Completed Date:  2013-10-01     Revised Date:  2013-10-17    
Medline Journal Info:
Nlm Unique ID:  101273794     Medline TA:  J Pediatr Neurosci     Country:  India    
Other Details:
Languages:  eng     Pagination:  154-7     Citation Subset:  -    
Affiliation:
Department of Pediatric Surgery, King Edward Memorial Hospital, Parel, Mumbai, India.
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