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Meckel-Gruber syndrome: A rare and lethal anomaly with review of literature
| Content Provider | Scilit |
|---|---|
| Author | Parelkar, Sandesh V. Kapadnis, Satish P. Joshi, Prashant B. Mundada, Dinesh Sanghvi, Beejal V. Oak, Sanjay N. |
| Copyright Year | 2013 |
| 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. 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. |
| Related Links | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3783728/pdf http://www.pediatricneurosciences.com/article.asp?issn=1817-1745;year=2013;volume=8;issue=2;spage=154;epage=157;aulast=Parelkar;type=2 |
| File Format | XHTML |
| ISSN | 18171745 |
| e-ISSN | 19983948 |
| DOI | 10.4103/1817-1745.117855 |
| Journal | Journal of Pediatric Neurosciences |
| Issue Number | 2 |
| Volume Number | 8 |
| Language | English |
| Publisher | Medknow |
| Access Restriction | Open |
| Subject Keyword | Pediatrics and Child Health Encephalocele Meckel-gruber Syndrome Polycystic Kidney Polydactyly Journal of Pediatric Neurosciences, Volume 8, Issue 2 |
| Content Type | Text |
| Resource Type | Article |
| Subject | Neuroscience Pediatrics, Perinatology and Child Health |