Ontology highlight
ABSTRACT:
SUBMITTER: Aquilano G
PROVIDER: S-EPMC9366515 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature
Aquilano Giulia G Linnér Agnes A Ygberg Sofia S Stödberg Tommy T Henckel Ewa E
Frontiers in pediatrics 20220728
Pyridoxine-dependent epilepsy is a rare autosomal recessive disease usually associated with neonatal seizures that do not respond to common antiseizure medications but are controlled by pyridoxine administration. Because the symptoms can mimic common neonatal disorders, the diagnosis can be initially missed or delayed. We report a fatal case of a boy who was initially diagnosed with respiratory distress, birth asphyxia, and persistent pulmonary hypertension and whose condition rapidly deteriorat ...[more]