Novel mutations in FLVCR1 cause tremors, sensory neuropathy with retinitis pigmentosa.
Zhenyu LiYize LiXujun ChuKang DuYuwei TangZhiying XieMeng YuJianwen DengHe LvWei ZhangZhaoxia WangLingchao MengYun YuanPublished in: Neuropathology : official journal of the Japanese Society of Neuropathology (2023)
The mutations of the feline leukemia virus subgroup C receptor-related protein 1 (FLVCR1) cause ataxia with retinitis pigmentosa. Recent studies indicated a large variation in the phenotype of FLVCR1-associated diseases. In this report, we describe an adult male who manifested first with tremors in his third decade, followed by retinitis pigmentosa, sensory ataxia, and sensory neuropathy in his fourth decade. While retinitis pigmentosa and sensory ataxia are well-recognized features of FLVCR1-associated disease, tremor is rarely described. Whole-exome sequencing revealed novel compound heterozygous pathogenic FLVCR1 variants: c.498 G > A; p.(Trp166*) and c.369 T > G; p.(Phe123Leu). In addition, we have highlighted the ultrastructural abnormalities of the sural biopsy in this patient.