Hemoglobin Himeji and inconsistent hemoglobin A1c values: a case report

Genetic Aspects of DiabetesPediatric Diabetes

Phenotypic variability in two siblings with monogenic diabetes due to the same ABCC8 gene mutation

Pediatr Diabetes.

Cattoni A, Jackson C, Bain M, Houghton J, Wei C

doi: 10.1111/pedi.

Genetic Aspects of Diabetes

Familial GATA6 mutation causing variably expressed diabetes mellitus and cardiac and renal abnormalities

Endocrinol Diabetes Metab Case Rep.

Du YT, Moore L, Poplawski NK, De Sousa SMC

doi: 10.1530/EDM-19-0022.

Diabetes - General

A glucokinase gene mutation in a young boy with diabetes mellitus, hyperinsulinemia, and insulin resistance

Int Med Case Rep J.

Emelyanov AO, Sechko E, Koksharova E, Sklyanik I, Kuraeva T, Mayorov A, Peterkova V, Dedov I

doi: 10.2147/IMCRJ.S125103.

Diabetes - General

Low HbA1c With Normal Hemoglobin in a Diabetes Patient Caused by PIEZO1 Gene Variant: A Case Report.

Front Endocrinol (Lausanne).

Song A, Lu L, Li Y, Lin M, Yuan X, Cheng X, Xia W, Wang O, Xing X

doi: 10.3389/fendo.2020.00356.

Diabetes - GeneralGlycemic Control

Emergence of insulin resistance following empirical glibenclamide therapy: a case report of neonatal diabetes with a recessive INS gene mutation

J Pediatr Endocrinol Metab.

Yildiz M, Akcay T, Aydin B, Akgun A, Dogan BB, De Franco E, Ellard S, Onal H

doi: 10.1515/jpem-2017-0325.

Diabetes - GeneralType 1 Diabetes

Subarachnoid and parencyhmal haemorrhages as a complication of severe diabetic ketoacidosis in a pre-adolescent with new onset type 1 diabetes

Pediatr Diabetes.

Finn BP, Power C, McSweeney N, Breen D, Wyse G, O'Connell SM

doi: 10.1111/pedi.12760.

Type 1 Diabetes

Case Report: Metreleptin Treatment in a Patient With a Novel Mutation for Familial Partial Lipodystrophy Type 3, Presenting With Uncontrolled Diabetes and Insulin Resistance

Front Endocrinol (Lausanne)

Lambadiari V, Kountouri A, Maratou E, Liatis S, Dimitriadis GD, Karpe F

doi: 10.3389/fendo.2021.684182

Diabetes - General

Case of disseminated pyomyositis in poorly controlled type 2 diabetes mellitus with diabetic ketoacidosis

J Diabetes Investig.

Tanabe A, Kaneto H, Kamei S, Hirata Y, Hisano Y, Sanada J, Irie S, Kinoshita T, Tatsumi F, Shimoda M, Kohara K, Mune T, Kaku K

doi: 10.1111/jdi.12393

Diabetes and Pregnancy

Caudal regression syndrome in a fetus of a glucokinase-maturity-onset diabetes of the young pregnancy

Diabet Med.

Taylor RAM, Mackie A, Mogra R, Pinner J, Rajendran S, Ross GP

doi: 10.1111/dme.13844.

Related content

Phenotypic variability in two siblings with monogenic diabetes due to the same ABCC8 gene mutation

Familial GATA6 mutation causing variably expressed diabetes mellitus and cardiac and renal abnormalities

A glucokinase gene mutation in a young boy with diabetes mellitus, hyperinsulinemia, and insulin resistance

Low HbA1c With Normal Hemoglobin in a Diabetes Patient Caused by PIEZO1 Gene Variant: A Case Report.

Emergence of insulin resistance following empirical glibenclamide therapy: a case report of neonatal diabetes with a recessive INS gene mutation

Subarachnoid and parencyhmal haemorrhages as a complication of severe diabetic ketoacidosis in a pre-adolescent with new onset type 1 diabetes

Case Report: Metreleptin Treatment in a Patient With a Novel Mutation for Familial Partial Lipodystrophy Type 3, Presenting With Uncontrolled Diabetes and Insulin Resistance

Case of disseminated pyomyositis in poorly controlled type 2 diabetes mellitus with diabetic ketoacidosis

Caudal regression syndrome in a fetus of a glucokinase-maturity-onset diabetes of the young pregnancy