Browsing by Author "Suriyawansa, D."

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    Meckel Gruber syndrome: a single gene cause of recurrent neural tube defects
    (Sri Lanka Medical Association, 2001) de Silva, D.; Suriyawansa, D.; Mangalika, M.; Samarasinghe, D.
    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.