A Rare Case of Neonatal Diabetes due to COQ2 Gene Mutation.

Authors :: Nazlı Gönç, E.
Çakır, Meltem
Düzova, Ali
Özaltın, Fatih
Alikaşifoğlu, Ayfer
Alev Özön, Z.
Kandemir, Nurgün
Source :: Journal of Clinical Research in Pediatric Endocrinology; 2015 Supplement, Vol. 7, p16-16, 1p
Publication Year :: 2015
Abstract: The article presents a case study of two siblings with neonatal diabetes due to coenzyme Q10 deficiency. The patients have no family history of diabetes, renal or neurological disorders. The clinical diagnosis of the patients' coenzyme Q10 deficiency was confirmed with the same mutation in COQ2 gene. The article also discusses the role of CoQ2 gene mutation in neonatal diabetes.