Yildiz Edibe Pembegül, Yesil Gözde, Bektas Gonca, Caliskan Mine, Tatlı Burak, Aydinli Nur, Ozmen Meral
Division of Pediatric Neurology, Department of Pediatrics, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey.
Department of Medical Genetics, Bezmi Alem Vakif University Faculty of Medicine, Istanbul, Turkey.
Clin Neurol Neurosurg. 2018 Jan;164:47-49. doi: 10.1016/j.clineuro.2017.11.008. Epub 2017 Nov 21.
Spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME), a rare disorder caused by mutation in the ASAH1 gene, is characterized by progressive muscle weakness and intractable epilepsy. The literature about SMA-PME is very rare and most of the time limited to case reports. Mutation in the ASAH1 gene is also found in another rare syndrome which is Farber disease. We report a case of a 13.5-year-old girl with SMA-PME associated with ASAH1 gene mutation. She presented with progressive muscle weakness, tremor, seizure, and cognitive impairment. Clinical features and electrophysiological investigations revealed a motor neuron disease and generalized epilepsy. The marked difference in disease manifestations may explain why Farber and SMA-PME diseases were not suspected of being allelic conditions. SMA-PME cases with ASAH1 mutation could be treated using therapeutic studies regarding Farber disease. In patients with undefined PME or lower motor neuron disease cases, ASAH1 mutation scans should be studied.
伴有进行性肌阵挛癫痫的脊髓性肌萎缩症(SMA-PME)是一种由ASAH1基因突变引起的罕见疾病,其特征为进行性肌肉无力和难治性癫痫。关于SMA-PME的文献非常罕见,大多数时候仅限于病例报告。在另一种罕见综合征——法伯病中也发现了ASAH1基因突变。我们报告一例13.5岁患有与ASAH1基因突变相关的SMA-PME的女孩。她表现为进行性肌肉无力、震颤、癫痫发作和认知障碍。临床特征和电生理检查显示为运动神经元病和全身性癫痫。疾病表现的显著差异可能解释了为什么法伯病和SMA-PME未被怀疑为等位基因疾病。伴有ASAH1突变的SMA-PME病例可采用针对法伯病的治疗研究进行治疗。对于未明确诊断的PME或下运动神经元病病例,应研究ASAH1基因突变扫描。