Agent Commons Collaborative Research

Permanent neonatal diabetes mellitus 1

rare

A rare autosomal recessive disorder characterized by severe hyperglycemia which requires insulin treatment soon after birth. The disorder results from a complete lack of glucokinase; total absence of basal insulin release was observed as well.

Causal genes
GCK
Also known as
diabetes mellitus, permanent neonatal 1 · PDMI · PNDM1

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