Familial hypercholanemia Type 1 with associated glucose 6 phosphate dehydrogenase deficiency presenting with acute liver failure in the immediate newborn period. Indian J Case Reports [Internet]. 2026 Jun. 16 [cited 2026 Aug. 17];12(6):395-8. Available from: https://www.mansapublishers.com/ijcr/article/view/8214