Genetic Analysis of 25 Patients with 5α-Reductase Deficiency in Chinese Population
Background. A deficiency in steroid 5α-reductase type 2 is an autosomal recessive disorder. Affected individuals manifested ambiguous genitalia, which is caused by decreased dihydrotestosterone (DHT) synthesis in the fetus. Methods. We analyzed 25 patients with 5α-reductase deficiency in China. Seve...
Main Authors: | Bing Han, Tong Cheng, Hui Zhu, Jie Yu, Wen-jiao Zhu, Huai-dong Song, Haijun Yao, Jie Qiao |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2020-01-01
|
Series: | BioMed Research International |
Online Access: | http://dx.doi.org/10.1155/2020/1789514 |
Similar Items
-
Identification of three novel SRD5A2 mutations in Chinese patients with 5α-reductase 2 deficiency
by: Tong Cheng, et al.
Published: (2019-01-01) -
Molecular Genetic Study of Dihydropteridine Reductase Deficient Hyperphenylalaninemia in Chinese
by: Pei-Fen Yen, et al.
Published: (2001) -
Genetic sequencing of a patient with Kallmann syndrome plus 5α-reductase type 2 deficiency
by: Wen Ji, et al.
Published: (2017-01-01) -
Growth Pattern in Chinese Children With 5α-Reductase Type 2 Deficiency: A Retrospective Multicenter Study
by: Xiu Zhao, et al.
Published: (2019-03-01) -
Genetic Variation of 25 Y-Chromosomal and 15 Autosomal STR Loci in the Han Chinese Population of Liaoning Province, Northeast China.
by: Jun Yao, et al.
Published: (2016-01-01)