Deficiency of androgen receptors in male pseudohermaphroditism

Erna Mark; Salvador Castells; Kenneth Glassberg; Sook J.A. Choi; Francisca Tolete-Velcek; Karen David; Claude J. Migeon

doi:10.1016/0090-4295(83)90017-1

Deficiency of androgen receptors in male pseudohermaphroditism

Erna Mark, Salvador Castells, Kenneth Glassberg, Sook J.A. Choi, Francisca Tolete-Velcek, Karen David, Claude J. Migeon

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

3 Scopus citations

Abstract

A diagnosis of androgen receptor deficiency was made in a male with ambiguous genitalia during the neonatal period. Since the neonate had a small hypospadiac phallus with laboratory evidence of a receptor deficiency and clinical unresponsiveness to high levels of androgen, it was decided to assign a female gender. Bilateral orchiectomy and phallic recession were performed.

Original language	English (US)
Pages (from-to)	168-171
Number of pages	4
Journal	Urology
Volume	21
Issue number	2
DOIs	https://doi.org/10.1016/0090-4295(83)90017-1
State	Published - Feb 1983
Externally published	Yes

ASJC Scopus subject areas

Urology

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10.1016/0090-4295(83)90017-1

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abstract = "A diagnosis of androgen receptor deficiency was made in a male with ambiguous genitalia during the neonatal period. Since the neonate had a small hypospadiac phallus with laboratory evidence of a receptor deficiency and clinical unresponsiveness to high levels of androgen, it was decided to assign a female gender. Bilateral orchiectomy and phallic recession were performed.",

author = "Erna Mark and Salvador Castells and Kenneth Glassberg and Choi, {Sook J.A.} and Francisca Tolete-Velcek and Karen David and Migeon, {Claude J.}",

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AU - Mark, Erna

AU - Castells, Salvador

AU - Glassberg, Kenneth

AU - Choi, Sook J.A.

AU - Tolete-Velcek, Francisca

AU - David, Karen

AU - Migeon, Claude J.

PY - 1983/2

Y1 - 1983/2

N2 - A diagnosis of androgen receptor deficiency was made in a male with ambiguous genitalia during the neonatal period. Since the neonate had a small hypospadiac phallus with laboratory evidence of a receptor deficiency and clinical unresponsiveness to high levels of androgen, it was decided to assign a female gender. Bilateral orchiectomy and phallic recession were performed.

AB - A diagnosis of androgen receptor deficiency was made in a male with ambiguous genitalia during the neonatal period. Since the neonate had a small hypospadiac phallus with laboratory evidence of a receptor deficiency and clinical unresponsiveness to high levels of androgen, it was decided to assign a female gender. Bilateral orchiectomy and phallic recession were performed.

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Deficiency of androgen receptors in male pseudohermaphroditism

Abstract

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