Difficulties in Diagnosis and Treatment of 5α-Reductase Type 2 Deficiency in a Newborn with 46,XY DSD-Reference-Cited by-同舟云学术

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Difficulties in Diagnosis and Treatment of 5α-Reductase Type 2 Deficiency in a Newborn with 46,XY DSD

Published:2010 Issue:1 Volume:74 Page:67-71
ISSN:1663-2826
Container-title:Hormone Research in Paediatrics
language:en
Short-container-title:Horm Res Paediatr

Author:

Walter Kerstin N.,Kienzle Frederike B.,Frankenschmidt Alexander,Hiort Olaf,Wudy Stefan A.,van der Werf-Grohmann Natascha,Superti-Furga Andrea,Schwab Karl Otfried

Publisher

S. Karger AG

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Cited by 51 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Variability in Sex Assignment at Birth and Etiological Diagnosis of Differences of Sex Development: A Ten-Year Institutional Experience from Assam;Indian Journal of Endocrinology and Metabolism;2024-07

2. 5‐Alpha reductase deficiency; an important cause of 46, XY DSD: Report of three cases within a family;Clinical Case Reports;2023-05

3. Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty;Endocrine Journal;2023

4. Genetic Variants in SRD5A2 in a Spectrum of DSD Patients from Australian Clinics Highlight Importance of Genetic Testing alongside Typical First-Line Investigations;Sexual Development;2023

5. Steroid 5α-reductase 2 deficiency;Genetic Steroid Disorders;2023

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