Unknown

Dataset Information

0

A case report of maturity-onset diabetes of the young (MODY12) in a Chinese Han patient with a novel ABCC8 gene mutation.


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

altmetric image

Publications

A case report of maturity-onset diabetes of the young (MODY12) in a Chinese Han patient with a novel ABCC8 gene mutation.

Wang Yuan Y   Kang Chao C   Tong Qiang Q   Wang Hui H   Zhang Rui R   Qiao Qiao Q   Sang Qian Q   Wang Xiaocui X   Wang Jian J   Xu Jing J  

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]

Similar Datasets

| S-EPMC7516341 | biostudies-literature
| S-EPMC5014798 | biostudies-literature
| S-EPMC9381955 | biostudies-literature
| S-EPMC8734027 | biostudies-literature
| S-EPMC9979303 | biostudies-literature
| S-EPMC10050546 | biostudies-literature
| S-EPMC8374143 | biostudies-literature