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Renton, A.E., Majounie, E., Waite, A., Simón-Sánchez, J., Rollinson, S., Gibbs, J.R., et al. (2011) A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD. Neuron, 72, 257-268.
https://doi.org/10.1016/j.neuron.2011.09.010

has been cited by the following article:

• TITLE: Familial Lateral Sclerosis with Juvenile Onset: About 3 Cases and Review of the Literature

  AUTHORS: Camara Mamady, Barry Souleymane Djigué, Dore Male, Toure Mohamed Lamine, Diallo Mohamed Tafsir, Toure Laïla, Youla Seny, Konate Ibrahimasory, Barry Louceny Fatoumata, Camara Mohamed Salif, Camara Idrissa, Doumbouya Idrissa, Djibo Hamani Bachir, Conde Mohamed Lamine, Cisse Fodé Abass

  KEYWORDS: ALS, Familial, Juvenile

  JOURNAL NAME: Journal of Biosciences and Medicines, Vol.11 No.10, October 11, 2023

  ABSTRACT: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease deadly. In Africa, little data exists on this condition and the form familial is the most common with a younger age of onset. Our observations relate to three brothers, born from a consanguineous marriage. The diagnosis of amyotrophic lateral sclerosis was certain placed in all patients according to the criteria of Awaji. The average age of patients was 16.66 years, and the average age of onset of symptoms was 10.33 years old. The female gender was the most represented with a sex ratio of 0.5. Our patients benefited from rilusole, vitamin D and physiotherapy. A only patient presented with dysphagia. However, no cases have been observed at this day.