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46,XY DSD due to 17β-HSD3 deficiency and 5α-reductase type 2 deficiency.

Advances in experimental medicine and biology - 1 Jan 2011

Inacio Marlene, Sircili Maria Helena P, Brito Vinicius N, Domenice Sorahia, Oliveira-Junior Ari Alves, Arnhold Ivo J P, Tibor Francisco D, Costa Elaine M F, Mendonca Berenice B

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Share to 17-Hydroxysteroid Dehydrogenases
Share to 3-Oxo-5-alpha-Steroid 4-Dehydrogenase
Share to Adolescent

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 21691945
DOI: 10.1007/978-1-4419-8002-1_3

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46,XY DSD due to 17β-HSD3 deficiency and 5α-reductase type 2 deficiency.PMID 21691945Read ↗

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46,XY Sex Development Defect due to a Novel Homozygous (Splice Site) c.673_1G>C Variation in the HSD17B3 Gene: Case ReportSemantic proximity Read ↗

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Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSDSemantic proximity Read ↗

Clinical and molecular spectrum of patients with 17β-hydroxysteroid dehydrogenase type 3 (17-β-HSD3) deficiency.Semantic proximity Read ↗

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