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Cholestatic Liver Failure and Hypoglycemia in a Newborn: A Mitochondrial Pathology due to Citrin Deficiency
Julien Neveu1, Mathilde Butori2, Anne Spraul3
1Department of Pediatric Neurology Hôpitaux Pédiatriques de Nice CHU-Lenval Nice France.
Abstract:
In an infant with cholestasis and recurrent hypoglycemia, the combination of hypercitrullinemia, hypermethioninemia, and hyperthreoninemia should prompt testing for citrin deficiency, because early metabolic and genetic diagnosis allows targeted nutritional treatment and rapid clinical improvement.
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