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Male Pseudohermaphroditism

Known as: Male Pseudohermaphroditisms, Pseudohermaphroditism, Male, Pseudohermaphroditisms, Male 
Hermaphroditism refers to a discrepancy between the morphology of the gonads and that of the external genitalia. In male pseudohermaphroditism, the… 
National Institutes of Health

Related topics

Related topics

7 relations

Broader (1)

46, XY Disorders of Sex Development
Congenital AbnormalityDenys-Drash SyndromeFemale PseudohermaphroditismFrasier Syndrome

Narrower (1)

MALE PSEUDOHERMAPHRODITISM: DEFICIENCY OF TESTICULAR 17,20-DESMOLASE

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
1999
Highly Cited
1999
Characteristics of a Highly Labile Human Type 5 17β-Hydroxysteroid Dehydrogenase1.
17β-Hydroxysteroid dehydrogenases (17βHSDs) play an essential role in the formation of active intracellular sex steroids. Six… 
Review
1994
Review
1994
Disorders of Steroid 17α-Hydroxylase Deficiency
Highly Cited
1992
Highly Cited
1992
Genetic and pharmacological evidence for more than one human steroid 5 alpha-reductase.
The enzyme steroid 5 alpha-reductase catalyzes the conversion of testosterone into the more potent androgen, dihydrotestosterone… 
Highly Cited
1985
Highly Cited
1985
Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia.
A six-month-old 46,XY infant with a female phenotype and ambiguous genitalia was evaluated for male pseudohermaphroditism. The… 
Highly Cited
1976
Highly Cited
1976
Dihydrotestosterone binding by cultured human fibroblasts. Comparison of cells from control subjects and from patients with hereditary male pseudohermaphroditism due to androgen resistance.
Dihydrotestosterone binding was measured in culture fibroblasts from 14 control subjects and from 12 patients with five different… 
Highly Cited
1976
Highly Cited
1976
Steroid 5alpha-reductase in cultured human fibroblasts. Biochemical and genetic evidence for two distinct enzyme activities.
Highly Cited
1974
Highly Cited
1974
Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndrome.
Abstract A family with incomplete male pseudohermaphroditism inherited as an apparent X-linked recessive trait was investigated… 
Highly Cited
1972
Highly Cited
1972
STEROID 17, 20‐DESMOLASE DEFICIENCY: A NEW CAUSE OF MALE PSEUDOHERMAPHRODITISM
In a child with male pseudohermaphroditism (ambiguous external genitalia, XY sex chromosomal constitution and normal… 
Highly Cited
1972
Highly Cited
1972
Studies on the pathogenesis of the pseudohermaphroditism in the mouse with testicular feminization.
The pathogenesis of the male pseudohermaphroditism in the mouse with X-linked testicular feminization (Tfm) has been investigated… 
Highly Cited
1970
Highly Cited
1970
Male Pseudohermaphroditism Due to 17a -Hydroxylase Deficiency
Abstract This is the first report of a male with 17α-hydroxylase deficiency resulting in male pseudohermaphroditism, ambiguous… 
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