Mutations in FUS are the most frequent genetic cause in juvenile sporadic ALS patients of Chinese origin

Abstract

Juvenile onset ALS is a very rare form of motor neuron disease, with the first symptoms of motor neuron degeneration manifested before 25 years of age. Mutations in the alsin (ALS2), senataxin (SETX), and spatacsin (SPG11) genes have been associated with familial ALS with juvenile onset and slow progression, whereas the genetic architecture of sporadic juvenile ALS remains unclear. We screened mutations in C9orf72, SOD1, FUS, TARDBP, ANG, VCP and PFN1 in 16 juvenile sporadic ALS patients. Four cases (25%) carrying FUS mutations and one individual (6%) harbouring a SOD1 mutation were identified. All cases had an aggressive disease course. Our results suggest that FUS mutations are the most frequent genetic cause in early-onset sporadic ALS patients of Chinese origin. Genetic testing of FUS should be performed in early-onset ALS patients especially those with an aggressive disease course.

Key words:

• Amyotrophic lateral sclerosis
• juvenile onset
• FUS
• SOD1

Acknowledgements

The authors thank the patients and their families, as well as the healthy control subjects, for their cooperation in this study.

Declaration of interest

The authors declare that they have no actual or potential conflicts of interest.

Supplementary material available online at http://dx.doi.org/10.3109/21678421.2016.1143012