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Up to: Multiple congenital anomalies/dysmorphic syndrome without intellectual disability · MKKS-related ciliopathy

McKusick-Kaufman syndrome

McKusick-Kaufman syndrome is a very rare, genetic developmental disorder presenting in the neonatal period characterized by genitourinary malformations, polydactyly, and more rarely, congenital heart disease or gastrointestinal malformations.

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This condition has no sub-types.