hrp0098p1-74 | Multisystem Endocrinology | ESPE2024
AL AzkawiHanan
, Nasser Nagla
, AL Yahyai Moza
, AL Madhani Shaima
Case 1: Twelve-year-old girl, presented with symptomatic hypoglycemia at the age of four. At six, she has type 1 diabetes mellitus (T1DM) started on insulin pump with excellent glycemic control. Genetic testing sent suspected MODY, revealed heterozygous variant in WFS1 gene, representing autosomal dominance inheritance. She screened for WFS associated disorder; negative.Case 2: Eighteen-year-old male with T1DM on insulin...