相关期刊:《Case Reports in Clinical Medicine》《World Journal of Clinical Cases》《Open Journal of Rheumatology and Autoimmune Diseases》《China Medical Abstracts(Internal Medicine)》更多>>
Supported by the Department of Education of Zhejiang Province,No.Y201738451;Health and Family Planning Commission of Zhejiang Province,No.2016148438
BACKGROUND Pseudohypoparathyroidism type Ia(PHP Ia) is a rare hereditary syndrome, and patients with early PHP Ia are generally not diagnosed based on the presentation of cutaneous nodules as the main clinical feature...