Hyperinsulinaemic Hypoglycaemia in Deoxyguanosine Kinase Deficiency.
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2019
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Abstract
Mutation in the deoxyguanosine kinase gene (DGUOK) results in hepatocerebral form of mitochondrial DNA (mtDNA)-depletion syndromes (MDS) . Affected individuals have early progressive liver failure, neurological abnormalities, hypoglycaemia and lactic acidosis. Majority of affected individuals die within the first year of life. Although hypoglycaemia is a consistent feature of hepatocerebral form of MDS, there is a single report of biochemical hyperinsulinism as the underlying cause with pancreatic islet cell hyperplasia on autopsy in two patients.
| Reference Key |
arya2019hyperinsulinaemicclinical
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|---|---|
| Authors | Arya, Ved Bhushan;Dhawan, Anil;Kapoor, Ritika R; |
| Journal | clinical endocrinology |
| Year | 2019 |
| DOI |
10.1111/cen.14084
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| URL | |
| Keywords | Keywords not found |
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