Familial hypercholanemia Type 1 with associated glucose 6 phosphate dehydrogenase deficiency presenting with acute liver failure in the immediate newborn period. Indian Journal of Case Reports, [S. l.], v. 12, n. 6, p. 395–398, 2026. DOI: 10.32677/ijcr.v12i6.8214. Disponível em: https://mansapublishers.com/ijcr/article/view/8214. Acesso em: 17 aug. 2026.