Meckel-Gruber syndrome

Kathmandu University Medical Journal

Volumn 4 NO. 3, Issue 15, 2006, Pages 334-336

  Ramachandran, U ^a   Malla, Tejesh ^a   Joshi, K S ^b  

^a MANIPAL TEACHING HOSPITAL   (Nepal)

^b Manipal Teaching Hospital ^*

Author keywords

Meningoencephalocoele; MKS syndrome

Indexed keywords

ARTICLE; AUTOSOMAL DISORDER; CASE REPORT; CHROMOSOME 17; CLINICAL FEATURE; HUMAN; IMAGING SYSTEM; KIDNEY POLYCYSTIC DISEASE; LUNG HYPOPLASIA; MALE; MECKEL SYNDROME; MENINGOCELE; MORTALITY; NEWBORN; NEWBORN CARE; POLYDACTYLY;

EID: 33846432045     PISSN: 18122027     EISSN: 18122078     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Smith's Recognizable Patterns of Human Malformations. 5h Ed WB Saunders Company 1997 Pages 184-185
2. Ahdab-Barmada M, Claassen D: A distinctive triad of malformations of the central nervous system in the Meckel-Gruber syndrome. J Neuropathol Exp Neurol 1990 Nov; 49(6): 610-20.
3. Color Atlas of Congenital Malformation Syndromes. Michael Baraitser, Robin M Winter, Mosby Wolfe 1996 Page 64
4. Paavola P, Salonen R, Baumer A: Clinical and genetic heterogeneity in Meckel syndrome. Hum Genet 1997 Nov; 101(1): 88-92.
5. Morgan NV, Gissen P, Sharif SM: A novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24. Hum Genet 2002 Oct; 111(4-5): 456-61.
6. Salonen R: The Meckel syndrome: clinicopathological findings in 67 patients. Am J Med Genet 1984 Aug; 18(4): 671-89.