[Clinical characteristics and molecular mechanisms of hypoparathyroidism related to GATA3 gene mutation].

Jing Yang、Y B Wang、Min Nie、Ying Jiang、Ming Li、Weibo Xia、Xiaoping Xing、O. Wang

2022PubMedBiochemistry, Genetics and Molecular Biology被引 2

摘要

Attention should be paid to genetic diseases in patients with childhood-onset hypoparathyroidism. The possibility of hypoparathyroidism-deafness-renal dysplasia syndrome should be considered in hypoparathyroidism patients with hearing loss or renal dysplasia. GATA3 gene screening is highly recommended for the confirmation of the diagnosis.

引用本文（GB/T 7714）

Jing Yang, Y B Wang, Min Nie, 等. [Clinical characteristics and molecular mechanisms of hypoparathyroidism related to GATA3 gene mutation].[J]. PubMed, 2022.

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DOI：https://doi.org/10.3760/cma.j.cn112138-20210519-00356

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