Clinical Characteristics, Molecular Features, and Long-Term Follow-Up of 15 Patients with Neonatal Diabetes: A Single-Centre Experience

Conclusion: Although the number of individuals born to consanguineous parents was considerably high in this cohort, KATP channel mutations (ABCC8/KCNJ11) were more common thanEIF2AK3 mutations (n = 6 vs.n = 1). Genetic analyses should be performed in all NDM cases due to the potential impact on treatment and prognosis.Horm Res Paediatr
Source: Hormone Research in Paediatrics - Category: Endocrinology Source Type: research