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 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.380 Dementia .
C10.228.140.380.266 Frontotemporal Lobar Degeneration .
C10.228.140.380.266.299 Frontotemporal Dementia .
C10.228.854 Spinal Cord Diseases .
C10.228.854.139 Amyotrophic Lateral Sclerosis .
C10.574 Neurodegenerative Diseases .
C10.574.562 Motor Neuron Disease .
C10.574.562.250 Amyotrophic Lateral Sclerosis .
C10.574.950 TDP-43 Proteinopathies .
C10.574.950.050 Amyotrophic Lateral Sclerosis .
C10.574.950.300 Frontotemporal Lobar Degeneration .
C10.574.950.300.299 Frontotemporal Dementia .
C10.668 Neuromuscular Diseases .
C10.668.467 Motor Neuron Disease .
C10.668.467.250 Amyotrophic Lateral Sclerosis .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.845 Proteostasis Deficiencies .
C18.452.845.800 TDP-43 Proteinopathies .
C18.452.845.800.050 Amyotrophic Lateral Sclerosis .
C18.452.845.800.300 Frontotemporal Lobar Degeneration .
C18.452.845.800.300.299 Frontotemporal Dementia .
F03 Mental Disorders .
F03.615 Neurocognitive Disorders .
F03.615.400 Dementia .
F03.615.400.380 Frontotemporal Lobar Degeneration .
F03.615.400.380.299 Frontotemporal Dementia .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Amyotrophic Lateral Sclerosis .
ALS (Amyotrophic Lateral Sclerosis) .
Amyotrophic Lateral Sclerosis With Dementia .
Amyotrophic Lateral Sclerosis, Guam Form .
Amyotrophic Lateral Sclerosis, Parkinsonism-Dementia Complex of Guam .
Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex 1 .
Charcot Disease .
Dementia With Amyotrophic Lateral Sclerosis .
Gehrig's Disease .
Guam Disease .
Guam Form of Amyotrophic Lateral Sclerosis .
Lou Gehrig's Disease .
Lou-Gehrigs Disease .
Amyotrophic Lateral Sclerosis Parkinsonism Dementia Complex 1 .
Amyotrophic Lateral Sclerosis, Parkinsonism Dementia Complex of Guam .
Disease, Guam .
Disease, Lou-Gehrigs .
Gehrig Disease .
Gehrigs Disease .
Sclerosis, Amyotrophic Lateral .
Lou Gehrig Disease .
Motor Neuron Disease, Amyotrophic Lateral Sclerosis .
GEHRIG'S DISEASE .
LOU GEHRIG'S DISEASE .
A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94) .
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Frontotemporal Dementia .
DDPAC .
Dementia, Frontotemporal .
Dementia, Frontotemporal, with Parkinsonism .
Dementia, Hereditary Dysphasic Disinhibition .
Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex .
Disinhibition-Dementia-Parkinsonism-Amytrophy Complex .
FTD-GRN .
FTD-PGRN .
FTDP-17 .
FTLD with TDP-43 Pathology .
FTLD-17 GRN .
FTLD-TDP .
Familial Pick's Disease .
Frontotemporal Dementia with Parkinsonism .
Frontotemporal Dementia with Parkinsonism-17 .
Frontotemporal Dementia, Ubiquitin-Positive .
Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions .
Frontotemporal Lobe Dementia .
Frontotemporal Lobe Dementia (FLDEM) .
GRN-Related Frontotemporal Dementia .
HDDD1 .
HDDD2 .
Hereditary Dysphasic Disinhibition Dementia .
Multiple System Tauopathy with Presenile Dementia .
Semantic Dementia .
Wilhelmsen-Lynch Disease .
Complex, Disinhibition-Dementia-Parkinsonism-Amyotrophy .
Complex, Disinhibition-Dementia-Parkinsonism-Amytrophy .
Complices, Disinhibition-Dementia-Parkinsonism-Amyotrophy .
Complices, Disinhibition-Dementia-Parkinsonism-Amytrophy .
Dementia, Frontotemporal Lobe .
Dementia, Frontotemporal Lobe (FLDEM) .
Dementia, GRN-Related Frontotemporal .
Dementia, Semantic .
Dementia, Ubiquitin-Positive Frontotemporal .
Dementias, Frontotemporal .
Dementias, Frontotemporal Lobe .
Dementias, Frontotemporal Lobe (FLDEM) .
Dementias, GRN-Related Frontotemporal .
Dementias, Semantic .
Dementias, Ubiquitin-Positive Frontotemporal .
Disease, Familial Pick's .
Disease, Wilhelmsen-Lynch .
Diseases, Familial Pick's .
Diseases, Wilhelmsen-Lynch .
Disinhibition Dementia Parkinsonism Amyotrophy Complex .
Disinhibition Dementia Parkinsonism Amytrophy Complex .
Disinhibition-Dementia-Parkinsonism-Amyotrophy Complices .
Disinhibition-Dementia-Parkinsonism-Amytrophy Complices .
FTLD with TDP 43 Pathology .
Familial Pick Disease .
Familial Pick's Diseases .
Familial Picks Disease .
Frontotemporal Dementia with Parkinsonism 17 .
Frontotemporal Dementia, GRN-Related .
Frontotemporal Dementia, Ubiquitin Positive .
Frontotemporal Dementias .
Frontotemporal Dementias, GRN-Related .
Frontotemporal Dementias, Ubiquitin-Positive .
Frontotemporal Lobar Degeneration With Ubiquitin Positive Inclusions .
Frontotemporal Lobe Dementias .
Frontotemporal Lobe Dementias (FLDEM) .
GRN Related Frontotemporal Dementia .
GRN-Related Frontotemporal Dementias .
Lobe Dementia, Frontotemporal .
Lobe Dementias, Frontotemporal .
Pick's Disease, Familial .
Pick's Diseases, Familial .
Semantic Dementias .
Ubiquitin-Positive Frontotemporal Dementia .
Ubiquitin-Positive Frontotemporal Dementias .
Wilhelmsen Lynch Disease .
Wilhelmsen-Lynch Diseases .
The most common clinical form of FRONTOTEMPORAL LOBAR DEGENERATION, this dementia presents with personality and behavioral changes often associated with disinhibition, apathy, and lack of insight. .
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