What is congenital hyperinsulinism? Definition, Meaning & Symptoms — Medical Dictionary
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congenital hyperinsulinism — Definition

Konjenital hiperinsülinizm / congenital hyperinsulinism
It is a rare disease characterized by excessive amount of insulin secretion from birth and beta cells of the pancreas. This condition leads to the normal drop of blood sugar (hyperemia). Usually occurs during newborn or infantity and may cause neurological damage if not treated. The underlying cause is usually genetic mutations and the severity of the disease varies from person.
Turkish
🇹🇷 Konjenital hiperinsülinizm
English
🇬🇧 congenital hyperinsulinism
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Frequently Asked Questions

❓ What is Konjenital hiperinsülinizm?
Konjenital hiperinsülinizm; it is a rare disease characterized by excessive amount of insulin secretion from birth and beta cells of the pancreas. This condition leads to the normal drop of blood sugar (hyperemia). Usually occurs during newborn or infantity and may cause neurological damage if not treated. The underlying cause is usually genetic mutations and the severity of the disease varies from person.
❓ What is congenital hyperinsulinism in Turkish?
The Turkish equivalent of "congenital hyperinsulinism" is Konjenital hiperinsülinizm.
❓ Which medical field is Konjenital hiperinsülinizm related to?
This term belongs to the Diseases category.