A Patient with Partial 17α-Hydroxylase Deficiency Initially Diagnosed with Asherman Syndrome and Pheochromocytoma-Reference-Cited by-同舟云学术

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A Patient with Partial 17α-Hydroxylase Deficiency Initially Diagnosed with Asherman Syndrome and Pheochromocytoma

Published:2024-01-31 Issue:1 Volume:65 Page:159-164
ISSN:1349-2365
Container-title:International Heart Journal
language:en
Short-container-title:Int. Heart J.

Author:

Yu Hongxiao¹,Liu Xiping²,Nie Zhihua¹,Xia Yanhua¹

Affiliation:

1. Haicang Hospital

2. Zhongshan Hospital of Xiamen University

Publisher

International Heart Journal (Japanese Heart Journal)

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

https://www.jstage.jst.go.jp/article/ihj/65/1/65_22-407/_pdf

Reference9 articles.

1. 1. Biglieri EG, Herron MA, Brust N. 17-hydroxylation deficiency in man. J Clin Invest 1966; 45: 1946-54.

2. 2. Chung BC, Picado-Leonard J, Haniu M, et al. Cytochrome P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase): cloning of human adrenal and testis cDNAs indicates the same gene is expressed in both tissues. Proc Natl Acad Sci U S A 1987; 84: 407-11.

3. 3. Won GS, Chiu CY, Tso YC, Jenq SF, Cheng PS, Jap TS. A compound heterozygous mutation in the CYP17 (17alpha-hydroxylase/17,20-lyase) gene in a Chinese subject with congenital adrenal hyperplasia. Metabolism 2007; 56: 504-7.

4. 4. Hwang DY, Hung CC, Riepe FG, et al. CYP17A1 intron mutation causing cryptic splicing in 17α-hydroxylase deficiency. PLoS One 2011; 6: e25492.

5. 5. Yanase T, Simpson ER, Waterman MR. 17 alpha-hydroxylase/17,20-lyase deficiency: from clinical investigation to molecular definition. Endocr Rev 1991; 12: 91-108.

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1. Congenital Adrenal Hyperplasia;International Heart Journal;2024-01-31

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