Jacob Francois-Dominique, Ho Eugenia S, Martinez-Ojeda Mayra, Darras Basil T, Khwaja Omar S
1Department of Neurology, Children's Hospital Boston and Harvard Medical School, Boston, MA.
J Child Neurol. 2013 Oct;28(10):1292-5. doi: 10.1177/0883073812454331. Epub 2012 Aug 21.
Dominant spinocerebellar ataxias are a rare clinically and genetically heterogeneous group of neurodegenerative disorders. They are characterized by progressive cerebellar ataxia resulting in unsteady gait, clumsiness, dysarthria, and swallowing difficulty. The onset of symptoms is usually in the third or fourth decade of life; however, more subtle clinical manifestations can start in early childhood. Spinocerebellar ataxia type 5, a dominant spinocerebellar ataxia associated with mutations involving β-III spectrin (SPTBN2), has been described in 3 families. It typically consists of a slowly progressive spinocerebellar ataxia with onset in the third decade. The authors present the first case of infantile-onset spinocerebellar ataxia associated with a novel SPTBN2 mutation (transition C>T at nucleotide position 1438), the proband having a much more severe phenotype with global developmental delay, hypotonia, tremor, nystagmus, and facial myokymia.
显性遗传性脊髓小脑共济失调是一类罕见的神经退行性疾病,在临床和基因方面具有异质性。其特征为进行性小脑共济失调,导致步态不稳、动作笨拙、构音障碍和吞咽困难。症状通常在生命的第三个或第四个十年开始出现;然而,更细微的临床表现可能在儿童早期就开始。5型脊髓小脑共济失调是一种与涉及β-III血影蛋白(SPTBN2)的突变相关的显性遗传性脊髓小脑共济失调,已在3个家系中被描述。它通常表现为在第三个十年开始的缓慢进行性脊髓小脑共济失调。作者报告了首例与一种新的SPTBN2突变(核苷酸位置1438处的C>T转换)相关的婴儿期起病的脊髓小脑共济失调,先证者具有更严重的表型,伴有全面发育迟缓、肌张力减退、震颤、眼球震颤和面部肌束震颤。