Hydrops fetalis in the McKusick-Kaufman syndrome: A case report

Robin S. Rosen; Maureen E. Bocian

doi:10.1016/0002-9378(91)90234-I

Hydrops fetalis in the McKusick-Kaufman syndrome: A case report

Robin S. Rosen, Maureen E. Bocian

Research output: Contribution to journal › Article › peer-review

14 Scopus citations

Abstract

McKusick-Kaufman syndrome is an autosomal recessive multiple malformation syndrome characterized by hydrometrocolpos and polydactyly. We report on a patient with McKusick-Kaufman syndrome and severe hydrops. This case illustrates the necessity of genetic evaluations for all patients with unexplained hydrops.

Original language	English (US)
Pages (from-to)	102-103
Number of pages	2
Journal	American journal of obstetrics and gynecology
Volume	165
Issue number	1
DOIs	https://doi.org/10.1016/0002-9378(91)90234-I
State	Published - Jul 1991

Keywords

McKusick-Kaufman syndrome
hydrometrocolpos
nonimmune hydrops

ASJC Scopus subject areas

Obstetrics and Gynecology

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10.1016/0002-9378(91)90234-I

Cite this

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title = "Hydrops fetalis in the McKusick-Kaufman syndrome: A case report",

abstract = "McKusick-Kaufman syndrome is an autosomal recessive multiple malformation syndrome characterized by hydrometrocolpos and polydactyly. We report on a patient with McKusick-Kaufman syndrome and severe hydrops. This case illustrates the necessity of genetic evaluations for all patients with unexplained hydrops.",

keywords = "McKusick-Kaufman syndrome, hydrometrocolpos, nonimmune hydrops",

author = "Rosen, {Robin S.} and Bocian, {Maureen E.}",

year = "1991",

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T2 - A case report

AU - Rosen, Robin S.

AU - Bocian, Maureen E.

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Y1 - 1991/7

N2 - McKusick-Kaufman syndrome is an autosomal recessive multiple malformation syndrome characterized by hydrometrocolpos and polydactyly. We report on a patient with McKusick-Kaufman syndrome and severe hydrops. This case illustrates the necessity of genetic evaluations for all patients with unexplained hydrops.

AB - McKusick-Kaufman syndrome is an autosomal recessive multiple malformation syndrome characterized by hydrometrocolpos and polydactyly. We report on a patient with McKusick-Kaufman syndrome and severe hydrops. This case illustrates the necessity of genetic evaluations for all patients with unexplained hydrops.

KW - McKusick-Kaufman syndrome

KW - hydrometrocolpos

KW - nonimmune hydrops

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IS - 1

ER -

Hydrops fetalis in the McKusick-Kaufman syndrome: A case report

Abstract

Keywords

ASJC Scopus subject areas

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