Ontology highlight
ABSTRACT: Rationale
Maturity onset diabetes of the young (MODY) is the most common type of monogenic diabetes, characterized by autosomal dominant inheritance, the age of onset is often <25 years old, and the clinical manifestations are atypical. MODY12 is caused by a rare missense mutation of adenosine triphosphate (ATP)-binding cassette transporter subfamily C member 8 (ABCC8) gene and more than 50 ABCC8 variants were associated with MODY12.Patient concerns
The patient was a 30-year-old Chinese Han man. He was overweight with a poor control of blood glucose.Diagnoses
The patient was diagnosed with MODY12.Interventions
The patient was given glimepiride (4 mg/d) with diet and exercise therapy to reduce blood glucose and weight.Outcomes
The level of fasting blood glucose and C-peptide was improved after 1 year treatment as well as body weight.Lessons
A Chinese Han adult with a heterozygous missense mutation c.3976G > A (p.Glu1326Lys) was diagnosed with MODY12, which was the new pathogenic mutation for the disease. This report expands the spectrum of variants causing MODY12 and reduces misdiagnosis.
SUBMITTER: Wang Y
PROVIDER: S-EPMC9750649 | biostudies-literature | 2022 Dec
REPOSITORIES: biostudies-literature

Medicine 20221201 49
<h4>Rationale</h4>Maturity onset diabetes of the young (MODY) is the most common type of monogenic diabetes, characterized by autosomal dominant inheritance, the age of onset is often <25 years old, and the clinical manifestations are atypical. MODY12 is caused by a rare missense mutation of adenosine triphosphate (ATP)-binding cassette transporter subfamily C member 8 (ABCC8) gene and more than 50 ABCC8 variants were associated with MODY12.<h4>Patient concerns</h4>The patient was a 30-year-old ...[more]