High incidence of hypertension-mediated organ damage in a series of Chinese patients with 17α-hydroxylase deficiency-Reference-Cited by-同舟云学术

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High incidence of hypertension-mediated organ damage in a series of Chinese patients with 17α-hydroxylase deficiency

Published:2022-01-14 Issue:1 Volume:76 Page:151-161
ISSN:1559-0100
Container-title:Endocrine
language:en
Short-container-title:Endocrine

Author:

Zhao Zhiyuan,Lu Lin,Wang Ou,Wu Xueyan,Sun Bang,Zhang Wei,Wang Xi,Mao Jiangfeng,Chen Shi,Tong Anli,Nie Min

Funder

National Natural Science Foundation of China

Natural Science Foundation of Beijing Municipality

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://link.springer.com/content/pdf/10.1007/s12020-021-02966-w.pdf

Reference38 articles.

1. D. EL-Maouche, W. Arlt, D.P. Merke, Congenital adrenal hyperplasia. Lancet 390(10108), 2194–2210 (2017)

2. C.E. Kater, E.G. Biglieri, Disorders of steroid 17 alpha-hydroxylase deficiency. Endocrinol. Metab. Clin. North Am. 23(2), 341–357 (1994)

3. W.L. Miller, R.J. Auchus, D.H. Geller, The regulation of 17,20 lyase activity. Steroids 62(1), 133–142 (1997)

4. B.C. Chung, J. Picado-Leonard, M. Haniu 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. 84(2), 407–411 (1987)

5. R.J. Auchus, Steroid 17-hydroxylase and 17,20-lyase deficiencies, genetic and pharmacologic. J. Steroid. Biochem. Mol. Biol. 165(Pt A), 71–78 (2017)

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1. 17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort;Endocrine;2024-07-17

2. CYP17A1 Pathogenic Variants in 26 Chinese Patients With 17α-Hydroxylase Deficiency by Targeted Long-Read Sequencing;The Journal of Clinical Endocrinology & Metabolism;2024-06-27

3. Single nucleotide polymorphism-based biomarker in primary hypertension;European Journal of Pharmacology;2024-06

4. Revealing a New Homozygous Variant in CYP17A1 c.908G>A (p. Gly303Asp) by Genotyping a Chinese Patient with 46, XY 17a-Hydroxylase/17,20-Lyase Deficiency and Adrenal Space-Occupying Lesion;Discovery Medicine;2024

5. Two Cases with 17-alpha Hydroxylase Deficiency Misdiagnosed as Primary Aldosteronism;Endocrine, Metabolic & Immune Disorders - Drug Targets;2023-09-07

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