1.
Ceylon Med J
; 2001 Mar; 46(1): 30
Article
in English
| IMSEAR
| ID: sea-47917
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.