Di Pisa Veronica, Cecconi Ilaria, Gentile Valentina, Di Pietro Elena, Marchiani Valentina, Verrotti Alberto, Franzoni Emilio
Child Neuropsychiatric Unit, Polyclinic S. Orsola-Malpighi, University of Bologna, Bologna, Italy.
J Child Neurol. 2012 Dec;27(12):1593-6. doi: 10.1177/0883073812436424. Epub 2012 Feb 28.
This article describes a case of pyruvate dehydrogenase deficiency in a 3-year-old boy who presented generalized hypotonia, severe psychomotor development delay, and generalized and partial seizures and was refractory to antiepileptic drugs. After the diagnosis, the patient was put on a ketogenic diet. Six months later, seizure frequency was reduced and psychomotor development had improved. At the same time he presented some side effects, such as 2 episodes of significant increases in cholesterol and triglycerides associated with viral respiratory infections. The latter decreased with a supplementation of ω-3 fatty acids and an increase in caloric intake.
本文描述了一名3岁男孩丙酮酸脱氢酶缺乏症的病例,该男孩出现全身性肌张力减退、严重精神运动发育迟缓、全身性和部分性癫痫发作,且对抗癫痫药物难治。诊断后,该患者采用了生酮饮食。6个月后,癫痫发作频率降低,精神运动发育有所改善。同时,他出现了一些副作用,如2次与病毒性呼吸道感染相关的胆固醇和甘油三酯显著升高。补充ω-3脂肪酸和增加热量摄入后,后者有所减轻。