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...

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Bibliografiset tiedot
Päätekijät: Stagi, Stefano, Lapi, Elisabetta, Pantaleo, Marilena, Chiarelli, Francesco, Seminara, Salvatore, de Martino, Maurizio
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2014
Aiheet:
Case Report
Linkit: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
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