Meckel Gruber syndrome: a single gene cause of recurrent neural tube defects

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DC Field	Value	Language
dc.contributor.author	de Silva, D.	en_US
dc.contributor.author	Suriyawansa, D.	en_US
dc.contributor.author	Mangalika, M.	en_US
dc.contributor.author	Samarasinghe, D.	en_US
dc.date.accessioned	2014-10-29T09:19:02Z	-
dc.date.available	2014-10-29T09:19:02Z	-
dc.date.issued	2001	en_US
dc.identifier.citation	The Ceylon Medical Journal; 46(1): pp.30	en_US
dc.identifier.issn	0009-0875 (Print)	en_US
dc.identifier.uri	http://repository.kln.ac.lk/handle/123456789/1470	-
dc.description.abstract	Meckel Gruber syndrome (MGS), an autosomal recessive disorder characterised by posterior encephalocoele, multicystic kidneys and post-axial polydactyly should be recognised by obstetricians and paediatricians to counsel parents regarding the 25% recurrence risk. We report a consanguineous family with MGS affecting three infants.	-
dc.publisher	Sri Lanka Medical Association	en_US
dc.title	Meckel Gruber syndrome: a single gene cause of recurrent neural tube defects	en_US
dc.type	Letter	en_US
dc.identifier.department	Paediatrics	en_US
dc.creator.corporateauthor	Sri Lanka Medical Association	en_US
dc.description.note	Comment: in Prenatal diagnosis of lethal congenital malformations in Sri Lanka. [Ceylon Med J. 2001]	-
Appears in Collections:	Journal/Magazine Articles

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