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Identification of Glucokinase Mutations in Subjects With Gestational Diabetes Mellitus

1 Jun 1993

Abstract excerpt

Recent studies have shown that mutations in the glucokinase gene on chromosome 7 can cause an autosomal dominant form of NIDDM with a variable clinical phenotype and onset during childhood. The variable clinical phenotype includes mild fasting hyperglycemia (i.e., a plasma glucose value of > 110 mg/dl, a value that is at least 2-3 SDs above normal), impaired glucose tolerance, gestational diabetes mellitus, as...

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PMID: 8495817
DOI: 10.2337/diab.42.6.937

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Related research

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Identification of Glucokinase Mutations in Subjects With Gestational Diabetes MellitusPMID 8495817Read ↗

Preliminary screening of mutations in the glucokinase gene of Chinese patients with gestational diabetes.Semantic proximity Read ↗

Identification of two new mutations in the glucokinase gene that result in maturity-onset diabetes of the young.Semantic proximity Read ↗

Glucokinase mutations in a phenotypically selected multiethnic group of women with a history of gestational diabetesSemantic proximity Read ↗

Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families.Semantic proximity Read ↗

Human glucokinase gene: isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin-dependent (type 2) diabetes mellitus.Semantic proximity Read ↗

A high prevalence of glucokinase mutations in gestational diabetic subjects selected by clinical criteria.Semantic proximity Read ↗

Diagnosis and management of glucokinase monogenic diabetes in pregnancy: current perspectivesSemantic proximity Read ↗

Recognition and Management of Individuals With Hyperglycemia Because of a Heterozygous Glucokinase Mutation.Semantic proximity Read ↗

Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia.Semantic proximity Read ↗

A novel heterozygous mutation in the glucokinase gene is responsible for an early-onset mild form of maturity-onset diabetes of the young, type 2.Semantic proximity Read ↗

Glucokinase (GCK) mutations in hyper- and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy.Semantic proximity Read ↗

Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus.Semantic proximity Read ↗

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