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Genetic aetiology of primary adrenal insufficiency in Chinese children.

Zhuo ChangWei LuZhuhui ZhaoLi XiXiaojing LiRong YeJinwen NiZhou PeiMiaoying ZhangRuoqian ChengZhangqian ZhengChengjun SunJing WuFei-Hong Luo
Published in: BMC medical genomics (2021)
We found ethnicity-based differences in the CYP21A2 gene variant spectrum among different study populations. Female 21-OHD patients tended to have higher 17-OHP and TES levels, which warrants caution in relation to the effects of virilization. Novel gene variants detected in the CYP21A2, NR0B1, AAAS and NNT genes expanded the genetic spectrum of PAI, however, further improvement of genetic testing tools beyond our protocol are still needed to uncover the complete aetiology of PAI in children.
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