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Last Updated: 10/31/2025
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Found 67 publications
5α Reductase Deficiency-a Rare Cause of Ambiguous Genitalia and Gender Dysphoria.
Journal: JCEM case reports
Published: June 18, 2024
Value of the human chorionic gonadotropin stimulation test in the diagnosis of disorder of sexual development in children
Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Published: March 04, 2024
Preimplantation genetic testing and prenatal diagnosis in a family with pseudovaginal perineoscrotal hypospadias: A case report.
Journal: Medicine
Published: November 21, 2023
In vitro functional study of fifteen SRD5A2 variants found in Chinese patients and the relation between the SRD5A2 genotypes and phenotypes.
Journal: The Journal of steroid biochemistry and molecular biology
Published: July 16, 2023
The Genotype-Phenotype Correlation in Human 5α-Reductase Type 2 Deficiency: Classified and Analyzed from a SRD5A2 Structural Perspective.
Journal: International journal of molecular sciences
Published: January 19, 2023
Genotype-phenotype correlations, surgical selections, and postoperative complications of 5α-reductase 2 deficiency in 69 children with hypospadias.
Journal: Asian journal of andrology
Published: December 01, 2022
Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty.
Journal: Endocrine journal
Published: October 10, 2022
Fertility potential in 5α-reductase type 2 deficient males.
Journal: Journal of pediatric urology
Published: May 07, 2022
Validation of steroid ratios for random urine by mass spectrometry to detect 5α-reductase deficiency in Vietnamese children.
Journal: Clinical chemistry and laboratory medicine
Published: March 22, 2022
Clinical, Hormonal, and Genetic Characteristics of 5α-Reductase Type 2 Deficiency in 103 Chinese Patients.
Journal: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
Published: February 12, 2022
Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD
Journal: Journal of clinical research in pediatric endocrinology
Published: February 09, 2022
Last Updated: 10/31/2025