Monogenic diabetes occurs in up to 3% of people with diabetes. Mutations in over 40
different genes are responsible. The most common genes affected are HNF1A, HNF4A …

Monogenic diabetes is frequently mistakenly diagnosed as either type 1 or type 2 diabetes,
yet accounts for approximately 1–2% of diabetes. Identifying monogenic forms of diabetes …

Abstract Purpose of Review Monogenic diabetes accounts for 1–2% of all diabetes cases,
but is frequently misdiagnosed as type 1, type 2, or gestational diabetes. Accurate genetic …

Pregnancy in women with monogenic diabetes is potentially complex, with significant
implications for both maternal and fetal health. Among these, maturity-onset diabetes of the …

Most diabetes is polygenic in etiology, with (type 1 diabetes, T1DM) or without (type 2
diabetes, T2DM) an autoimmune basis. Genetic counseling for diabetes generally focuses …

Monogenic diabetes represents a heterogeneous group of disorders resulting from defects
in single genes. Defects are categorized primarily into two groups: disruption of β‐cell …

Monogenic diabetes includes several clinical conditions generally characterized by early-
onset diabetes, such as neonatal diabetes, maturity-onset diabetes of the young (MODY) …

Monogenic diabetes mellitus, which is diabetes caused by a defect in a single gene that is
associated with β cell function or insulin action, accounts for 1% to 6% of all pediatric …

The genetic architecture of diabetes mellitus in general and in pregnancy is complex, owing
to the multiple types of diabetes that comprise both complex/polygenic forms and monogenic …

Monogenic diabetes results from inheritance of one or more mutations in a single gene and
accounts for 1–3% of diabetes cases diagnosed< 30 years. Mutations may be inherited in a …