Referenced in: none

Automatically associated channels: Kir1.1 , Kir6.2

Title: AV59M KCNJ11 gene mutation leading to intermediate DEND syndrome in a Chinese child.

Authors: Yanmei Sang, Guichen Ni, Yi Gu, Min Liu

Journal, date & volume: J. Pediatr. Endocrinol. Metab., 2011 , 24, 763-6

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/22145471

Abstract
Heterozygous activating mutations in the KCNJ11 gene can cause permanent and transient neonatal diabetes. In the present study, we sequenced the KCNJ11 gene in a Chinese boy diagnosed with permanent neonatal diabetes mellitus (PNDM) and also in his parents. A heterozygous 175G > A (V59M) mutation was identified in the patient, while no KCNJ11 gene mutations were found in his parents, indicating that this mutation is de novo. The patient with the V59M mutation successfully switched from insulin injections to oral glibenclamide; 2 years of follow-up revealed that the patient had intermediate developmental delay, epilepsy and neonatal diabetes (DEND) syndrome. This is the first patient who is reported to have iDEND syndrome due to KCNJ11 V59M mutation in China.