Lipiński Patryk, Ciara Elżbieta, Bogdańska Anna, Jurkiewicz Elżbieta, Tylki-Szymańska Anna
Institute of Clinical Sciences, Maria Skłodowska-Curie Medical Academy, Plac Żelaznej Bramy 10, 00-136, Warsaw, Poland.
Department of Medical Genetics, Children's Memorial Health Institute, Warsaw, Poland.
J Appl Genet. 2025 May 17. doi: 10.1007/s13353-025-00974-4.
L-2-hydroxyglutaric aciduria (L-2-HGA, #236,792) is an autosomal recessive neurodegenerative disorder caused by the deficiency of L-2-hydroxyglutarate dehydrogenase, a flavin adenine dinucleotide (FAD)-dependent enzyme, due to biallelic pathogenic variants in the L2HGDH gene. The present study described the patient with L2HGA presenting with a slight psychomotor delay, epilepsy from 5 years of age, non-progressive cerebellar ataxia, and mild to moderate intellectual disability during 10 years of follow-up. Two different heterozygous variants in the L2HGDH gene were identified in the patient: a known substitution c.829C > T(p.Arg277*) and a novel substitution c.1196 + 1G > A corresponding with significantly increased urinary L-2-hydroxyglutarate (L2HG) excretion. A 6-month period of treatment with riboflavin (100 mg/day) was implemented with no clinical nor biochemical effect.
L-2-羟基戊二酸尿症(L-2-HGA,#236,792)是一种常染色体隐性神经退行性疾病,由L-2-羟基戊二酸脱氢酶缺乏引起,该酶是一种黄素腺嘌呤二核苷酸(FAD)依赖性酶,病因是L2HGDH基因的双等位基因致病性变异。本研究描述了一名L2HGA患者,该患者在10年随访期间表现出轻微精神运动发育迟缓、5岁起患癫痫、非进行性小脑共济失调以及轻度至中度智力残疾。在该患者中鉴定出L2HGDH基因的两种不同杂合变异:一种已知的替换c.829C>T(p.Arg277*)和一种新的替换c.1196+1G>A,这与尿L-2-羟基戊二酸(L2HG)排泄显著增加相对应。实施了为期6个月的核黄素(100毫克/天)治疗,未产生临床或生化效果。