Zaridoust Ahya, Rabbani Ali, Sayarifard Fatemeh, Thiel Christian T, Rezaei Nima
Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Iran J Pediatr. 2013 Jun;23(3):363-5.
Insulin resistance syndromes are a heterogeneous group of disorders with variable clinical phenotypes, associated with increased blood glucose and insulin levels.
Herein, a 10-year old girl with abnormal face and dentition is presented. She has suffered from diabetes mellitus type I since she was 6 years old. Hyperglycemia did not respond to age appropriate insulin dosage; therefore, insulin dosage was increased, but did not lead to appropriate glycemic control. Twenty two exons of insulin receptor gene (INSR), on short arm of chromosome 19, were sequenced, but no identifiable disease causing mutation was detected.
Although a rare mutation within the intronic or promoter region has not been excluded in this case, further molecular studies on patients with insulin resistance syndromes associated with certain features are needed.
胰岛素抵抗综合征是一组具有不同临床表型的异质性疾病,与血糖和胰岛素水平升高有关。
本文介绍了一名面部和牙列异常的10岁女孩。她自6岁起就患有1型糖尿病。高血糖对适合其年龄的胰岛素剂量无反应;因此,增加了胰岛素剂量,但并未实现适当的血糖控制。对位于19号染色体短臂上的胰岛素受体基因(INSR)的22个外显子进行了测序,但未检测到可识别的致病突变。
尽管该病例未排除内含子或启动子区域存在罕见突变的可能性,但仍需要对具有某些特征的胰岛素抵抗综合征患者进行进一步的分子研究。