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Dictionary » Persistent Hyperinsulinemia Hypoglycemia of Infancy
 

Persistent Hyperinsulinemia Hypoglycemia of Infancy

Introduction: Persistent Hyperinsulinemia Hypoglycemia of Infancy

Description of Persistent Hyperinsulinemia Hypoglycemia of Infancy

Persistent Hyperinsulinemia Hypoglycemia of Infancy: A form of nontransient HYPOGLYCEMIA, unique to infancy, due to autosomal recessive mutations of the sulfonylurea receptor gene on CHROMOSOME 11. Defects in the sulfonylurea receptors (ATP-BINDING CASSETTE TRANSPORTERS) on the PANCREATIC BETA CELLS prevent negative feedback of GLUCOSE-regulated INSULIN release thus resulting in HYPERINSULINEMIA. Clinical phenotype includes SEIZURES; COMA; and often large BIRTH WEIGHT for GESTATIONAL AGE.
Source: MeSH 2007

Persistent Hyperinsulinemia Hypoglycemia of Infancy: Related Topics

These medical condition or symptom topics may be relevant to medical information for Persistent Hyperinsulinemia Hypoglycemia of Infancy:

Hierarchical classifications of Persistent Hyperinsulinemia Hypoglycemia of Infancy

The following list attempts to classify Persistent Hyperinsulinemia Hypoglycemia of Infancy into categories where each line is subset of the next.

MeSH 2007 Hierarchy:

MeSH 2007 Hierarchy

MeSH 2007 Hierarchy

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

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