McKusick-kaufman syndrome: a rare case report with review of literature

ABSTRACT

Hydrometrocolpos [HMC], postaxial polydactyly [PAP] and congenital heart disease [CHD] are well documented features of the McKusick Kaufman Syndrome [MKKS]. This is a rare autosomal recessive disease which may be associated with other multiple malformations. MKKS is an extremely rare cause of non-immune hydrops with only one case reported in the literature. We report the first case of MKKS in Kuwait who presented with non-immune hydrops