Facial onset amyotrophic lateral sclerosis with K3E variant in the Cu/Zn superoxide dismutase gene
Facial onset amyotrophic lateral sclerosis with K3E variant in the Cu/Zn superoxide dismutase gene
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面部发病的肌萎缩侧索硬化症,伴有铜/锌超氧化物歧化酶基因 K3E 变异
DOI:
10.1080/21678421.2020.1797092
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发表时间:
2020
影响因子:
2.8
通讯作者:
Kuwabara Satoshi
中科院分区:
文献类型:
--
作者:
Shibuya Kazumoto;Sawai Setsu;Sugiyama Atsuhiko;Koide Mizuho;Nishiyama Ayumi;Aoki Masashi;Kuwabara Satoshi
We describe a 48-year-old man, suffering from difficulties in closing his eyes. He subsequently experienced progressive weakness in the facial and bulbar regions and upper limbs. His father and paternal grandmother had limb weakness as initial manifestations and were diagnosed with amyotrophic lateral sclerosis (ALS). In the present case, neuroimaging and laboratory studies were unremarkable, and neurophysiological studies disclosed diffuse denervation. Genetic testing identified a heterozygous c.10A>G, p.K4E (K3E) variant in superoxide dismutase 1 (SOD1) gene, and he was diagnosed with familial ALS. In ALS, facial muscles are rarely involved as an initial symptom. The present patient is a first case of facial onset ALS with K3E variant inSOD1gene. Two case reports identified facial palsy as an initial manifestation in familial ALS with C6G variant inSOD1gene. Several ALS patients with variants inSOD1gene may have facial onset history.
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影响因子:
0.4
作者:
M. Mizuno;Y. Ueki;K. Sakurai;K. Okita;F. Endo;K. Yamanaka;M. Morita;N. Matsukawa
通讯作者:
N. Matsukawa
影响因子:
2.8
作者:
M. Kuźma;M. Berdyński;M. Morita;Yuji Takahashi;A. Kawata;K. Kaida;Beata Kaźmierczak;A. Łusakowska;J. Goto;S. Tsuji;C. Żekanowski;H. Kwiecinski
通讯作者:
H. Kwiecinski
影响因子:
11
作者:
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通讯作者:
Lauria, Giuseppe
影响因子:
4.2
作者:
Nishiyama, Ayumi;Niihori, Tetsuya;Aoki, Masashi
通讯作者:
Aoki, Masashi