Article
Genetics of neonatal hyperinsulinism.
Archives of disease in childhood. Fetal and neonatal edition - 1 Mar 2000
Glaser B, Thornton P, Otonkoski T, Junien C
Abstract excerpt
Congenital hyperinsulinism (HI) is a clinically and genetically heterogeneous entity. The clinical heterogeneity is manifested by severity ranging from extremely severe, life threatening disease to very mild clinical symptoms, which may even be difficult to identify. Furthermore, clinical responsiveness to medical and surgical management is extremely variable. Recent discoveries have begun to clarify the...
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