Corcia Philippe, Danel Veronique, Lacour Arnaud, Beltran Stephane, Andres Christian, Couratier Philippe, Blasco Helene, Vourc'h Patrick
a Centre de Ressources et de Compétences SLA, CHU Tours , France.
b Fédération des Centres de Ressources et de Compétences de Tours et Limoges, Litorals , France.
Amyotroph Lateral Scler Frontotemporal Degener. 2017 May;18(3-4):298-301. doi: 10.1080/21678421.2016.1265564. Epub 2017 Jan 5.
Although amyotrophic lateral sclerosis (ALS) typically occurs around 60 years, numerous publications report an onset of ALS before the age of 25 years that define juvenile ALS (jALS). Over the last decade, growing literature mentioned jALS with an aggressive evolution which are mainly linked to the FUS gene. We report here the case of a 25-year-old woman with a bulbar onset ALS that progressed in less than 12 months to invasive ventilation due to respiratory failure; Genetic screening identified a new mutation in the FUS gene that lies within the last codon. After reading the literature, it might be legitimate to consider that jALS linked to FUS mutations represent a specific entity different from both classical jALS and adult ALS linked to FUS gene. This should encourage clinician to firstly screen the FUS gene in the presence of a sporadic ALS that occurs before the age of 25 and with an aggressive profile of evolution.
尽管肌萎缩侧索硬化症(ALS)通常在60岁左右发病,但大量文献报道了25岁之前发病的ALS,即青少年型ALS(jALS)。在过去十年中,越来越多的文献提到jALS病情进展迅速,主要与FUS基因有关。我们在此报告一例25岁女性,以延髓起病的ALS,在不到12个月内因呼吸衰竭进展为有创通气;基因筛查在FUS基因的最后一个密码子处发现了一个新突变。查阅文献后,可以合理地认为与FUS突变相关的jALS是一种不同于经典jALS和与FUS基因相关的成人ALS的特殊实体。这应促使临床医生在遇到25岁之前散发发病且病情进展迅速的ALS时,首先对FUS基因进行筛查。