期刊
FRONTIERS IN ENDOCRINOLOGY
卷 12, 期 -, 页码 -出版社
FRONTIERS MEDIA SA
DOI: 10.3389/fendo.2021.524242
关键词
Bloom syndrome; diabetes; short stature; azoospermia; leptin
资金
- National Key Research and Development Program of China [2018YFC2001100, 2016YFC0901500]
- Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences [CIFMS2017-I2M-1-008]
Bloom syndrome (BS) is a rare autosomal recessive disorder, with only one reported case without diabetes in the Chinese population. This study presented the first case of BS with diabetes in China, identifying a new pathogenic variant in the BLM gene and highlighting BS as a rare cause of diabetes in the Chinese population.
Bloom syndrome (BS) is a rare autosomal recessive disorder that causes several endocrine abnormalities. So far, only one BS pedigree, without diabetes, has been reported in the Chinese population. We presented the first case of BS with diabetes in the Chinese population and explored the clinical spectrum associated with endocrine. Possible molecular mechanisms were also investigated. Our study indicated that BS may be one rare cause of diabetes in the Chinese population. We also found a new pathogenic sequence variant in BLM (BLM RecQ like helicase gene)(NM_000057.4) c.692T>G, which may expand the spectrum of BLM variants.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据