A brief report on juvenile amyotrophic lateral sclerosis cases in the United States National ALS Registry: 2010–2018
Affiliates | Jaime Raymond [1], Jasmine Berry [1], Edward J. Kasarskis [2], Theodore Larson [1], D. Kevin Horton [1] and Paul Mehta [1]
Received 04 Aug 2023, Accepted 20 Sep 2023, Published online: 03 Oct 2023 [1] Agency for Toxic Substances and Disease Registry/Centers for Disease Control and Prevention, Atlanta, GA, USA |
Journal | Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration |
Summary | This paper describes the demographic characteristics of Juvenile ALS (jALS), designated as presenting ALS symptoms before age 25, in the United States between 2010 and 2018. Forty-four cases of were identified in National ALS Registry data, of which the majority were non-white and male. More research is needed to better understand risk factors contributing to jALS, which could lead to earlier diagnosis and therapeutic interventions. |
Link to paper | Read the paper here! |