The prenatal diagnosis of the 48,xxyy syndrome

Paul E. Bibbins; Robert L. Anderson; Jack M. Rary; Howard W. Jones

doi:10.1002/pd.1970020208

The prenatal diagnosis of the 48,xxyy syndrome

Paul E. Bibbins, Robert L. Anderson, Jack M. Rary, Howard W. Jones

School of Medicine

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

Abstract

A 48,XXYY fetus was diagnosed prenatally in a 34‐year old female who was seen at 18‐5 weeks of pregnancy for genetic counselling and amniocentesis for advanced maternal age. The pregnancy was terminated, and skin and peripheral blood samples were obtained at the time of delivery. These samples also exhibited the 48,XXYY chromosomal complement.

Original language	English (US)
Pages (from-to)	123-125
Number of pages	3
Journal	Prenatal Diagnosis
Volume	2
Issue number	2
DOIs	https://doi.org/10.1002/pd.1970020208
State	Published - Jan 1 1982

Keywords

48,XXYY Klinefelter
Cryptochidism Aggressive behaviour
Prenatal Diagnosis
Syndrome Variant

ASJC Scopus subject areas

Obstetrics and Gynecology
Genetics(clinical)

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10.1002/pd.1970020208

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AB - A 48,XXYY fetus was diagnosed prenatally in a 34‐year old female who was seen at 18‐5 weeks of pregnancy for genetic counselling and amniocentesis for advanced maternal age. The pregnancy was terminated, and skin and peripheral blood samples were obtained at the time of delivery. These samples also exhibited the 48,XXYY chromosomal complement.

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The prenatal diagnosis of the 48,xxyy syndrome

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

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