The Journal of Contemporary Dental Practice

Register      Login

SEARCH WITHIN CONTENT

FIND ARTICLE

Volume / Issue

Online First

Archive
Related articles

VOLUME 13 , ISSUE 5 ( September-October, 2012 ) > List of Articles

CASE REPORT

Meckel-Gruber Syndrome (Dysencephalia Splanchnocystica)

B Prasanna Shetty, Nandakishore Alva

Citation Information : Shetty BP, Alva N. Meckel-Gruber Syndrome (Dysencephalia Splanchnocystica). J Contemp Dent Pract 2012; 13 (5):713-715.

DOI: 10.5005/jp-journals-10024-1214

Published Online: 01-10-2012

Copyright Statement:  Copyright © 2012; Jaypee Brothers Medical Publishers (P) Ltd.


Abstract

How to cite this article

Shetty BP, Alva N, Patil S, Shetty R. Meckel- Gruber Syndrome (Dysencephalia Splanchnocystica). J Contemp Dent Pract 2012;13(5):713-715.


PDF Share
  1. Beschreibung zweier durch sehr ahnliche Bildungsabweichung entsteller Geschwister. Dtsch Arch Physiol 1822;7:99.
  2. Beitrage zur Frage ‘gekoppelter’ missbildungen (Akrocephalosyndactylie und Dysencephalia splanchnocystica). Beitr Pathol Anat 1934;93:459.
  3. The Meckel syndrome (dysencephalia splanchnocystica, the Gruber syndrome). Birth Defects 1969;5:167.
  4. Meckel syndrome: What are the minimum diagnostic criteria? J Med Genet 1994 Jun;31(6):482-85.
  5. A novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24. Hum Genet 2002 Oct;111(4-5):456-61.
  6. Molecular pathology and genetics of congenital hepatorenal fibrocystic syndrome. J Med Genet 2003 May;40(5):311-19.
  7. Prenatal diagnosis of the Meckel-Gruber syndrome from 11th to 20th gestational week. Ultraschall Med 2004 Aug;25(4):275-79.
  8. Magnetic resonance imaging in fetal anomalies: What does it add to 3D and 4D US? Eur J Radiol 2009 Apr;74(1):250-55.
  9. An immunohistochemical study of human fetal liver in the Meckel-Gruber syndrome. Pathology 2005 Apr;37(2):137-43.
  10. Meckel-Gruber syndrome: Pathologic manifestations, minimal diagnostic criteria, and differential diagnosis. Arch Pathol Lab Med 2006 Aug;130(8):1236-38.
  11. Molecular diagnostics of Meckel-Gruber syndrome highlights phenotypic differences between MKS1 and MKS3. Hum Genet 2007 Jun;121(5):591-99.
  12. Mutations of the CEP290 gene encoding a centrosomal protein cause Meckel-Gruber syndrome. Hum Mutat 2008 Jan;29(1):45-52.
PDF Share
PDF Share

© Jaypee Brothers Medical Publishers (P) LTD.