Atypical clinical course of FXTAS: Rapidly progressive dementia as the major symptom

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Veröffentlicht in:	Neurology 2007-05, Vol.68 (21), p.1864-1866
Hauptverfasser:	GONCALVES, M. R. R, CAPELLI, L. P, NITRINI, R, BARBOSA, E. R, PORTO, C. S, LUCATO, L. T, VIANNA-MORGANTE, A. M
Format:	Artikel
Sprache:	eng
Schlagworte:	Age of Onset Aged Atrophy - etiology Atrophy - pathology Atrophy - physiopathology Biological and medical sciences Brain - pathology Brain - physiopathology Cognition Disorders - diagnosis Cognition Disorders - genetics Cognition Disorders - physiopathology Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Dementia - diagnosis Dementia - genetics Dementia - physiopathology Disease Progression Disorders of higher nervous function. Focal brain diseases. Central vestibular syndrome and deafness. Brain stem syndromes Fatal Outcome Fragile X Mental Retardation Protein - genetics Fragile X Syndrome - diagnosis Fragile X Syndrome - genetics Fragile X Syndrome - physiopathology Gait Ataxia - diagnosis Gait Ataxia - genetics Humans Magnetic Resonance Imaging Male Medical sciences Movement Disorders - diagnosis Movement Disorders - genetics Movement Disorders - physiopathology Nervous system (semeiology, syndromes) Neurology Time Factors
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