肌萎缩侧索硬化
医学
进行性肌萎缩
家族史
萎缩
吞咽困难
弱点
怀孕
疾病
儿科
病理
解剖
内科学
外科
遗传学
生物
作者
Lisette Bazán‐Rodríguez,Jesús A. Ruíz-Avalos,Oscar Bernal-López,Edmar Benitez-Alonso,Jesica Villaseñor-Sánchez,Francisca Fernández‐Valverde,Steven Vargas‐Cañas
出处
期刊:Neurocase
[Informa]
日期:2022-05-04
卷期号:28 (3): 323-330
被引量:3
标识
DOI:10.1080/13554794.2022.2100265
摘要
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease. In 10% the disease is familial and rarely occurs in childbearing age women. A 28-year-old female pregnancy patient presented a two-month history of dropped head syndrome, dysphagia, muscle weakness, atrophy, and lingual wasting. Electromyography supported the diagnosis of ALS. Due to family history and background, we carried out molecular genetic testing. We identified a novel variant of uncertain significance: c. 1566 G > C (p.Arg522Ser) in exon 15 in FUS gene. Our findings provide the first case of ALS onset during pregnancy with a novel mutation in FUS gene reported in Mexico.
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