Jung Jin Ho, Seo Jung Hwa, Lee Sukyoon, Heo Young Jin, Kim Donghyun, Chung Eun Joo, Oh Seong-Il
Department of Neurology, Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
Dementia and Neurodegenerative Disease Research Center, Inje University, Busan, Korea.
J Mov Disord. 2022 Jan;15(1):71-74. doi: 10.14802/jmd.21091. Epub 2021 Dec 24.
Despite recent advances in next-generation sequencing, the underlying etiology of adult-onset leukoencephalopathy has been difficult to elucidate. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a representative hereditary adult-onset leukoencephalopathy associated with vasculopathy. Leukoencephalopathy in spastic paraplegia type 4 (SPG4) is known to be rare, but it might be underestimated because most spastic paraplegia with leukoencephalopathy is rarely considered. We report a case of co-occurring SPG4 and CADASIL. A 61-year-old male presented with sudden visual impairment after a headache. He showed a spastic gait and had a family history with similar symptoms. An SPG4 gene mutation and a pathogenic variant in the NOTCH3 gene were found. This case shows that the diverse and complex clinical manifestations of patients with extensive leukoencephalopathy are related to more than one gene mutation. We also suggest the necessity for relevant genetic tests in the diagnosis of adult-onset leukoencephalopathy.
尽管下一代测序技术最近取得了进展,但成人起病的白质脑病的潜在病因一直难以阐明。伴有皮质下梗死和白质脑病的脑常染色体显性动脉病(CADASIL)是一种与血管病变相关的典型遗传性成人起病的白质脑病。已知痉挛性截瘫4型(SPG4)中的白质脑病很罕见,但可能被低估了,因为大多数伴有白质脑病的痉挛性截瘫很少被考虑到。我们报告一例SPG4和CADASIL同时发生的病例。一名61岁男性在头痛后突然出现视力障碍。他表现出痉挛性步态,并有类似症状的家族史。发现了SPG4基因突变和NOTCH3基因的致病变异。该病例表明,广泛白质脑病患者多样复杂的临床表现与不止一种基因突变有关。我们还建议在成人起病的白质脑病诊断中进行相关基因检测的必要性。