We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
A young‐onset type 2 diabetic Chinese girl with familial renal glycosuria caused by a novel mutation in SLC5A2: A case report.
- Authors
Qu, Yuqing; Hao, Limei; Wang, Xianling
- Abstract
Herein we described the clinical characteristics of a Chinese girl with youth-onset type 2 diabetes coexisting with FRG, in whom a novel mutation (NM 003041.4:c.1129 + 2 T > C) of the I SLC5A2 i gene might explain FRG occurrence. MODY is a special type of diabetes mellitus, representing a small but very important fraction of diabetic patients (1%-5%),[[4]] and 1%-6% of cases in pediatric age.[6] In this patient, no mutations in 14 genes associated with MODY have been detected, and its diagnosis was also excluded. The pathogenesis of youth-onset type 2 diabetes is different from that of maturity-onset diabetes of the young (MODY) and from type 1 diabetes, but there are many overlapped clinical manifestations among these three types of diabetes. A young-onset type 2 diabetic Chinese girl with familial renal glycosuria caused by a novel mutation in SLC5A2: A case report.
- Subjects
HYPERGLYCEMIA; URINARY tract infections; MATURITY onset diabetes of the young; GENETIC variation; GENETIC mutation; HUMAN biology; HEREDITY
- Publication
Journal of Diabetes, 2023, Vol 15, Issue 7, p622
- ISSN
1753-0393
- Publication type
Article
- DOI
10.1111/1753-0407.13410