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A rare case of 17 alpha-hydroxylase/17, 20-lyase deficiency: Clinical and genetic findings and follow-up outcomes

Dai, LZ; Ma, H; Ke, JF; Lin, CS; Huang, YL; Tian, Y; Chen, DL

Ma, H (通讯作者)，Xiamen Univ, Dept Endocrinol, Zhongshan Hosp, 209 Hubin South Rd, Xiamen 361004, Fujian, Peoples R China.

WOMENS HEALTH, 2022; 18 ():

Abstract

Here, we reported a case of a 16-year-old Chinese female patient (46, XX) diagnosed as 17 alpha-hydroxylase/17, 20-lyase deficiency (17-OHD) in June 2......

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