Disease Information for Benign familial tremor

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Clinical Manifestations
Signs & Symptoms
Abnormal movements/involuntary
Action Tremor
Alcohol improves tremor/temporaily
Fine tremor hands/head/not legs
Hand tremors
Handwriting progressive decline
Head tremor/fine
Hyperkinetic Movement Disorder
Involuntary Leg Movement Standing
Movement disorder/clears in sleep status
Postural tremor/resisting gravity
Tremor
Tremor 5-7 cps (hertz) frequency
Tremor ceases in sleep
Tremor in Elderly
Tremor, symmetrical
Tremor,fine
Tremor,intention
Tremor/fatigue increased
Tremor/stress increased
Tremulous speech
Tremulousness
Apparently well Silent disorder possible
Otherwise well Isolated problem
Disease Progression
Course/Benign course/disorder
Course/Chronic disorder
Course/Chronic only
Course/No sequelae expected
Course/Progressive/slowly chronic illness
Demographics & Risk Factors
Population Group
Child
Middle Age Adult
Population/Pediatrics population
Family History
Family history/Nerve disease
Family history/Tremor
Sex & Age Groups
Population/Adult Aged Only
Population/Adult/all
Population/Child
Population/Children/all
Population/Fifties adult
Population/Middle-aged adult
Population/Thirties adult
Associated Diseases & Rule outs
Rule Outs
Parkinsons disease
Associated Disease & Complications
Alcoholism/Chronic alcoholism
Benign familial tremor
Disease Synergy - Causes
Risk factor/Alcoholism
Disease Mechanism & Classification
Class
CLASS/Neurologic (category)
Pathophysiology
Pathophysiology/FET1 gene/on long arm chromosome 3 (3q13)
Pathophysiology/Gene locus 2.1
Pathophysiology/Gene locus 2p25-p22
Pathophysiology/Gene locus 3q13
Pathophysiology/Gene locus Chromosome 2
Pathophysiology/Gene locus chromosome 3
Pathophysiology/Gene Locus chromosome 3q
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Hereditary disease/Adult manifestations
Pathophysiology/Kindred gene ETM2/short arm chromosome 2 (2p22-25)
Pathophysiology/Several gene loci possible/kindred
Pathophysiology/Sporadic/hereditary/process
Pathophysiology/Maternal Chromosome mutation
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/Hereditofamilial (category)
PROCESS/Vegetative-Autonomic/Endocrine (category)
PROCESS/Hyperkinetic Movement disorders
Synonyms
Synonym
Benign, Benign familial tremor, Benign familial tremor (finding), Essential tremor (hereditary), familial tremor, Familial Tremors, Hereditary essential tremor, hereditary tremor, Heredofamilial tremor, tremor familial, tremor hereditary, TREMOR HEREDITARY BENIGN, Tremors Familial, Synonym/Benign essential tremor syndrome, Synonym/Benign intentional tremor, Synonym/Presenile tremor syndrome
Treatment
Drug Therapy - Indication
RX/Acetazolamide (Diamox)
RX/Alprazolam (Xanax)
RX/Atenolol (Tenormin)
RX/Beta-blocker
RX/Carbonic anhydrase inhibitor
RX/Clonidine (Catapres)
RX/Primidone (Mysoline)
RX/Propranolol (Inderal)
Other Treatments
TX/Avoid caffeine
Definition
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External Links Related to Benign familial tremor
Google
Wikipedia
Merck
Images
PubMed (National Library of Medicine)
NGC (National Guideline Clearinghouse)
Medscape (eMedicine)
Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)
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