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Updated: Aug 15, 2026

A Hyperandrogenic Mouse Model to Study Polycystic Ovary Syndrome
Published on: October 2, 2018
[Abnormalities of adrenal steroidogenesis in Chilean boys with micropenis]
Jorge Sapunar1, Teresa Vidal, Karin Bauer
1Unidad de Endocrinología, Departamento de Medicina Interna, Facultad de Medicina, Universidad de La Frontera, Temuco, Chile. medinter@ufro.cl
Background:
Mutations in type II 3 beta hydroxysteroid Dehydrogenase (3 beta HSD) are found in male children with severe undervirilized genitalia. Mild undervirilization (isolated micropenis or with distal hypospadia) can be associated with a partial deficit in 3 beta HSD activity.
Aim:
To assess the frequency of abnormal adrenal response to ACTH, suggesting a deficit in adrenal enzymatic activity, in children with mild undervirilization.
Patients And Methods:
We studied 26 male children with micropenis, aged one to eight years. Children with evidences of puberal development or in treatment with drugs that affect steroidal metabolism were excluded from the study. Serum levels of androstenedione (A), dehydroepiandrosterone (DHEA), progesterone (P), 17 hydroxyprogesterone (17 P) and the ratios DHEA/A, P/17 P, 17 P/DHEA were measured after an adrenal stimulation with 0.25 mg/m2 intramuscular ACTH.
Results:
Two children had DHEA y DHEA/A values suggesting a defective 3 beta HSD activity. Other two children had high levels of 17 P, suggesting a deficiency of cytochrome p450c21. A CYP 21 gene mutation was found in one of the later children.
Conclusions:
A low proportion of children with micropenis have a deficient 3 beta HSD activity.
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