Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype

BACKGROUND: Deletion of the subtelomeric region of 1p36 is one of the most common subtelomeric deletion syndromes. In monosomy 1p36, the presence of obesity is poorly defined, and glucose metabolism deficiency is rarely reported. However, the presence of a typical Prader-Willi-like phenotype in pati...

全面介紹

Na minha lista:
書目詳細資料
Main Authors: Stagi, Stefano, Lapi, Elisabetta, Pantaleo, Marilena, Chiarelli, Francesco, Seminara, Salvatore, de Martino, Maurizio
格式: Artigo
語言:Inglês
出版: BioMed Central 2014
主題:
Case Report
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC3916307/
https://ncbi.nlm.nih.gov/pubmed/24479866
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-15-16
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!

相似書籍