| 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] |
|