Further Delineation of the McKusick-Kaufman Hydrometrocolpos-Polydactyly Syndrome

David Chitayat, Sue Y.E. Hahm, Robert W. Marion, Gay S. Sachs, Dina Goldman, R. Gordon Hutcheon, Robert Weiss, Sangho Cho, Harold M. Nitowsky

Research output: Contribution to journalArticlepeer-review

32 Scopus citations


Six cases of the McKusick-Kaufman syndrome (MKS), including two cases that were diagnosed prenatally, were studied. Review of the 54 previously described cases indicates that postaxial polydactyly and hydrometrocolpos in female patients are the hallmark features of this entity. Other manifestations, such as malformations of gastrointestinal, cardiovascular, and ophthalmic structures, occur less consistently. Affected children require careful medical follow-up. Recurrence of hydrometrocolpos following surgical repair may lead to serious sequelae, such as chronic renal failure. We believe that MKS Is a distinct panethnic genetic entity, inherited in an autosomal recessive fashion, and that the diagnosis should be made only in female patients with hydrometrocolpos and polydactyly or in male patients with polydactyly who have an affected female relative.

Original languageEnglish (US)
Pages (from-to)1133-1136
Number of pages4
JournalAmerican Journal of Diseases of Children
Issue number10
StatePublished - Oct 1987

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health


Dive into the research topics of 'Further Delineation of the McKusick-Kaufman Hydrometrocolpos-Polydactyly Syndrome'. Together they form a unique fingerprint.

Cite this