Article
A novel GNAS mutation inherited from probable maternal mosaicism causes two siblings with pseudohypoparathyroidism type 1A.
Journal of pediatric endocrinology & metabolism : JPEM - 25 Sept 2020
Wang Qi, Xian Jiayi, Chen Pingjiao, Wang Jingying, Gao Yan, Zheng Xinyao, Tan Zhongkai, Li Changxing, Zeng Kang
Abstract excerpt
Objectives Objectives Pseudohypoparathyroidism type 1A (PHP1A) is caused by maternal inheritance of GNAS mutations. It is characterized by the resistance to several hormones, primarily the parathyroid hormone (PTH), and the features of Albright's hereditary osteodystrophy. Case presentation Here, we present a family comprised two affected brothers with PHP1A and identify a novel mutation (c.277C>T) in the GNAS...
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