Monogenic β-cell dysfunction in children: Clinical phenotypes, genetic etiology and mutational pathways
Monogenic diabetes accounts for 1-2% of all cases of diabetes mellitus and presentation is often in childhood. Recognizing the clinical features of monogenic β-cell dysfunction prevents misdiagnosis and allows for more effective management and genetic counseling. Monogenic β-cell dysfunction is a di...
Главные авторы: | Waterfield, T, Gloyn, A |
---|---|
Формат: | Journal article |
Язык: | English |
Опубликовано: |
2008
|
Схожие документы
-
Mutations in HHEX are not a common cause of monogenic forms of beta cell dysfunction.
по: Minton, J, и др.
Опубликовано: (2007) -
Defining the genetic aetiology of monogenic diabetes can improve treatment.
по: Gloyn, A, и др.
Опубликовано: (2006) -
Monogenic disorders of the pancreatic β-cell: Personalizing treatment for rare forms of diabetes and hypoglycemia
по: van de Bunt, M, и др.
Опубликовано: (2007) -
Vagus nerve stimulation in children with drug-resistant epilepsy of monogenic etiology
по: Han Xie, и др.
Опубликовано: (2022-09-01) -
Evidence That the Etiology of Congenital Hypopituitarism Has a Major Genetic Component but Is Infrequently Monogenic
по: Youn Hee Jee, и др.
Опубликовано: (2021-08-01)