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Novel glucokinase gene mutation in the first Macedonian family tested for MODY

Publication at Second Faculty of Medicine |
2017

Abstract

We present a boy with mild hyperglycemia detected during an upper respiratory infection. Novel splicing mutation in the intron 1 of the GCK gene (c.45+1G>A) was detected, and was subsequently confirmed in his father.

This is the first case of genetically confirmed Macedonian family with MODY.