Case Report: Extent of the Clinical Spectrum for C9orf72 Mutation - From Frontotemporal Dementia to Autonomic Dysfunction

• Главные авторы: Catherine Takeda-Raguin (Автор), Pierre Olivier Lang (Автор), Jérémie Perisse (Автор), Nathalie Philippi (Автор), Patrick Karcher (Автор), Thomas Vogel (Автор)
• Формат: ‌
• Опубликовано: Archive of Gerontology and Geriatrics Research - Peertechz Publications, 2017-01-24.
• Предметы: Case Report
• Online-ссылка: Connect to this object online.

<p>C9ORF72 gene mutation on chromosome 9 corresponding to a repetition of hexanucleotides (GGGGCC) xn is the most common mutation found in frontotemporal lobar dementia (FTLD) and amyotrophic lateral sclerosis (SLA) [1]. FTLD is characterized by an insidious onset with gradual evolution, a dec...