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Novel mutations in FLVCR1 cause tremors, sensory neuropathy with retinitis pigmentosa.
Li, Zhenyu; Li, Yize; Chu, Xujun; Du, Kang; Tang, Yuwei; Xie, Zhiying; Yu, Meng; Deng, Jianwen; Lv, He; Zhang, Wei; Wang, Zhaoxia; Meng, Lingchao; Yuan, Yun.
Afiliación
  • Li Z; Department of Neurology, Peking University First Hospital, Beijing, China.
  • Li Y; Department of Neurology, Peking University First Hospital, Beijing, China.
  • Chu X; Department of Neurology, Peking University First Hospital, Beijing, China.
  • Du K; Department of Neurology, Qujing First People's Hospital, Qujing, China.
  • Tang Y; Department of Neurology, Peking University First Hospital, Beijing, China.
  • Xie Z; Department of Neurology, Peking University First Hospital, Beijing, China.
  • Yu M; Department of Neurology, Peking University First Hospital, Beijing, China.
  • Deng J; Department of Neurology, Peking University First Hospital, Beijing, China.
  • Lv H; Department of Neurology, Peking University First Hospital, Beijing, China.
  • Zhang W; Department of Neurology, Peking University First Hospital, Beijing, China.
  • Wang Z; Department of Neurology, Peking University First Hospital, Beijing, China.
  • Meng L; Beijing Key Laboratory for Neurovascular Disease Discovery, Peking University First Hospital, Beijing, China.
  • Yuan Y; Key Laboratory for Neuroscience, National Health Commission of the People's Republic of China, Peking University, Beijing, China.
Neuropathology ; 44(2): 87-95, 2024 Apr.
Article en En | MEDLINE | ID: mdl-37469134
ABSTRACT
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.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Retinitis Pigmentosa / Enfermedades del Sistema Nervioso Periférico Límite: Adult / Humans / Male Idioma: En Revista: Neuropathology Asunto de la revista: NEUROLOGIA / PATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Retinitis Pigmentosa / Enfermedades del Sistema Nervioso Periférico Límite: Adult / Humans / Male Idioma: En Revista: Neuropathology Asunto de la revista: NEUROLOGIA / PATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China