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

• Main Authors: Catherine Takeda-Raguin (Author), Pierre Olivier Lang (Author), Jérémie Perisse (Author), Nathalie Philippi (Author), Patrick Karcher (Author), Thomas Vogel (Author)
• Format: Book
• Published: Archive of Gerontology and Geriatrics Research - Peertechz Publications, 2017-01-24.
• Subjects: Case Report
• Online Access: 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...