Aquilano Giulia, Linnér Agnes, Ygberg Sofia, Stödberg Tommy, Henckel Ewa
Department of Neonatology, Karolinska University Hospital, Stockholm, Sweden.
Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.
Front Pediatr. 2022 Jul 28;10:940103. doi: 10.3389/fped.2022.940103. eCollection 2022.
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 deteriorated during the first day of life.
维生素B6依赖型癫痫是一种罕见的常染色体隐性疾病,通常与新生儿惊厥有关,这些惊厥对常见的抗癫痫药物无反应,但通过给予维生素B6可得到控制。由于症状可能类似于常见的新生儿疾病,最初可能会漏诊或延误诊断。我们报告了一例致命病例,一名男婴最初被诊断为呼吸窘迫、出生窒息和持续性肺动脉高压,其病情在出生后的第一天迅速恶化。