Journal
FRONTIERS IN ENDOCRINOLOGY
Volume 12, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fendo.2021.524242
Keywords
Bloom syndrome; diabetes; short stature; azoospermia; leptin
Categories
Funding
- National Key Research and Development Program of China [2018YFC2001100, 2016YFC0901500]
- Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences [CIFMS2017-I2M-1-008]
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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.
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