Jaeger Bregje, Langeveld Mirjam, Brunkhorst Robert, Distelmaier Felix, Pop Ana, Wolf Nicole I, Bosch Annet M
Department of Child Neurology Emma Children's Hospital, Amsterdam University Medical Centers Amsterdam The Netherlands.
Department of Endocrinology and Metabolism Amsterdam University Medical Centers Amsterdam The Netherlands.
JIMD Rep. 2024 Jun 27;65(4):233-238. doi: 10.1002/jmd2.12427. eCollection 2024 Jul.
Riboflavin transporter deficiency (RTD) is a genetic disorder of reduced riboflavin (vitamin B2) uptake that causes progressive, multifocal neurological dysfunction. Most patients present in early childhood; if patients present later in life, symptoms usually develop more gradually. We report three previously healthy young adults, who developed rapidly progressive neurological symptoms after decreasing dietary intake of meat and dairy. After a diagnostic odyssey, the diagnosis of a riboflavin transporter deficiency was made. Treatment with high dose oral riboflavin (20-40 mg/kg/day) partially reversed symptoms. This case series highlights that reduced riboflavin intake as a result of dietary changes can unmask RTD at a later age. We emphasize the importance of early recognition of this progressive and potentially lethal disease and show that timely treatment with high dose riboflavin is highly effective.
核黄素转运体缺乏症(RTD)是一种因核黄素(维生素B2)摄取减少而导致的遗传性疾病,会引起进行性、多灶性神经功能障碍。大多数患者在幼儿期发病;如果患者在成年后发病,症状通常发展得较为缓慢。我们报告了三名此前健康的年轻人,他们在减少肉类和奶制品的饮食摄入后,迅速出现了进行性神经症状。经过漫长的诊断过程,最终确诊为核黄素转运体缺乏症。高剂量口服核黄素(20 - 40毫克/千克/天)治疗使症状部分得到缓解。该病例系列突出表明,饮食变化导致的核黄素摄入量减少可在较晚年龄引发RTD。我们强调早期识别这种进行性且可能致命疾病的重要性,并表明高剂量核黄素的及时治疗非常有效。