A Recessive Mutation in the Insulin Gene in Neonatal Diabetes
Neonatal diabetes mellitus (DM) is a persistent hyperglycemia occurring in the first 4-6 weeks of life that lasts more than two weeks and requires insulin for management. We report a case of a 23-day-old boy with neonatal diabetes due to recessive inheritance INS promoter C-331 C>A mutation accom...
Main Authors: | Abdulmoein Eid Al-Agha, Ihab Abd Al-hameed Ahmad, Faten Adnan Abdullah Basnawi, Elaf Yahia Faraj AL-Nasser |
---|---|
Format: | Article |
Language: | English |
Published: |
Turkiye Klinikleri
2015-03-01
|
Series: | Turkish Journal of Endocrinology and Metabolism |
Subjects: | |
Online Access: | http://dx.doi.org/10.4274/tjem.2326 |
Similar Items
-
Identification of insulin gene variants in patients with neonatal diabetes in the Chinese population
by: Junling Fu, et al.
Published: (2020-05-01) -
A homozygous mutation in the insulin gene () causing autosomal recessive neonatal diabetes in Saudi families
by: Adnan Al Shaikh, et al.
Published: (2020-03-01) -
Effect of Elevated Ketone Body on Maternal and Infant Outcome of Pregnant Women with Abnormal Glucose Metabolism During Pregnancy
by: Qian M, et al.
Published: (2020-11-01) -
A challenging diagnosis of B-ketothiolase deficiency mimicking type 1 diabetes mellitus
by: Amal Ali Al-Hakami, et al.
Published: (2021-01-01) -
Neonatal diabetes mutations disrupt a chromatin pioneering function that activates the human insulin gene
by: Ildem Akerman, et al.
Published: (2021-04-01)