A Japanese patient with a 2p25.3 terminal deletion presented with early‐onset obesity, intellectual disability and diabetes mellitus: A case report. Issue 2 (31st August 2021)

• Record Type: Journal Article
• Authors: Sakaue, Taka‐aki; Obata, Yoshinari; Fujishima, Yuya; Kozawa, Junji; Otsuki, Michio; Yamamoto, Toshiyuki; Maeda, Norikazu; Nishizawa, Hitoshi; Shimomura, Iichiro
• Is Part Of: Journal of diabetes investigation. Volume 13:Issue 2(2022)
• Page Start: 391
• Page End: 396
• Publication Date: 2021-08-31
• Subjects: 2p25.3 deletion -- Obesity -- Diabetes mellitus; Diabetes -- Periodicals; Diabetes -- Research -- Periodicals; Diabetes Mellitus -- Periodicals; 616.462005
• DOI: 10.1111/jdi.13645
• Languages: English
• ISSNs: 2040-1116

Abstract

ABSTRACT: 2p25.3 deletion syndrome is a rare genetic disorder that accompanies various phenotypic features, including early‐onset obesity and intellectual disability. Here, we report the first Japanese case of this deletion associated with severe obesity and diabetes mellitus. Microarray‐based comparative genomic hybridization analysis identified a 3.1‐Mb deletion of distal chromosome band 2p25.3, which was suspected as de novo. The patient also presented bilateral cataracts and adolescent‐onset muscular weakness of the upper limbs, both of which were uncommon in previously reported cases. It is possible that these symptoms are also important clinical features suggestive of this syndrome. Abstract : 2p25.3 deletion syndrome is a rare genetic disorder that accompanies various phenotypic features, including early‐onset obesity and intellectual disability. We report the first Japanese case of this deletion associated with severe obesity and diabetes mellitus, who presented uncommon features of bilateral cataracts and adolescent‐onset muscular weakness of the upper limbs.