Hyperinsulinism due to INSR deficiency

Orpha code: 263458OMIM code: 609968

Definition

A rare autosomal dominant form of familial hyperinsulinism characterized clinically by postprandial hypoglycemia, fasting hyperinsulinemia, and an elevated serum insulin-to-C peptide ratio, and a variable age of onset.

Disease data
Classification

Disease

Synonyms
Hyperinsulinemic hypoglycemia due to INSR deficiency
Hipoglikemia hiperinsulinemiczna z powodu niedoboru INSR
Hipoglikemia hiperinsulinemiczna z powodu niedoboru receptora insulinowego
Hyperinsulinemic hypoglycemia due to insulin receptor deficiency
ORPHA code
263458
OMIM code
609968
ICD10 code
E16.1
ICD11 code
-

No additional description.

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