de Silva, D.Suriyawansa, D.Mangalika, M.Samarasinghe, D.2014-10-292014-10-292001The Ceylon Medical Journal; 46(1): pp.300009-0875 (Print)http://repository.kln.ac.lk/handle/123456789/1470Meckel 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.Meckel Gruber syndrome: a single gene cause of recurrent neural tube defectsLetterPaediatrics