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Episodic Ataxia
Episodic ataxia
Overview
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Channelopathy
Spinocerebellar ataxia type-6
Familial hemiplegic migraine
Neurological disorders
(18)
Ataxia
Dyschronometria
Spinocerebellar ataxia
Cerebellar ataxia
Friedreich ataxia
Friedreich ataxia
DRPLA
Dysarthria
Machado-joseph disease
Neuromyotonia
Alternating hemiplegia of childhood
Fragile X
Olivoponto- cerebellar atrophy
Cadasil
Epilepsy
Arnold chiari malformation
Neuronal ceroid lipofuscinosis
Spinocerebellar ataxia type-6
Familial hemiplegic migraine
more...
Genetic disorders
(18)
Spastic ataxia
Galactosialidosis
Pyruvate dehydrogenase deficiency
Spinal muscular atrophy
Ataxia telangiectasia
Ataxia telangiectasia
Joubert syndrome
Genetic disorder
Polydactyly
Spinocerebellar ataxia type-6
Spinocerebellar ataxia
Friedreich ataxia
DRPLA
Familial hemiplegic migraine
Machado-joseph disease
Alternating hemiplegia of childhood
Channelopathies
Fragile X
Cadasil
more...
Neurology
(12)
Sensory ataxia
Paroxysmal
Episodic memory
Choreoathetosis
Epilepsies, partial
Epilepsies, partial
Movement disorders
Dystonia
Postural instability
Neurological disorders
Spastic ataxia
Joubert syndrome
Epilepsy
more...
Disability
Mental retardation
Neurological disorders
Spinocerebellar ataxia
Dysarthria
Fragile X
Medical terms
Diseases and disorders
Migraine with aura
Epilepsy
Ion channels
(9)
KCNA1
CACNA1A
Potassium channel
Calcium channel
KCNC3
KCNC3
Voltage-gated
Voltage-gated potassium channel
Voltage gated calcium channel
Channelopathies
more...
Rare diseases
Epidermolysis bullosa
Epidermolysis bullosa simplex
Galactosialidosis
Neuronal ceroid lipofuscinosis
Diseases and disorders
(36)
Episodic ataxia syndrome
Myokymia
Cerebellar agenesis
Gait ataxia
Cerebellar degeneration
Cerebellar degeneration
Acidemia
Aplastic
Hypersensitivity
Neurological disorders
Ataxia
Friedreich ataxia
Spastic ataxia
Sialidosis
Galactosialidosis
Pyruvate dehydrogenase deficiency
Symptoms
Machado-joseph disease
Spinal muscular atrophy
Physiologic nystagmus
Alternating hemiplegia of childhood
Fragile X
Ataxia telangiectasia
Joubert syndrome
Movement disorders
Epidermolysis bullosa simplex
Olivoponto- cerebellar atrophy
Dystonia
Cadasil
Polydactyly
Epilepsy
Ectodermal dysplasia
Coloboma
Arnold chiari malformation
Neuronal ceroid lipofuscinosis
Inborn error of metabolism
Mental retardation
more...
Calcium channel
Hypokalemic periodic paralysis
Malignant hyperthermia
Timothy syndrome
Familial hemiplegic migraine
Potassium channel
Inward-rectifier potassium ion channel
Isaacs syndrome
Jervell and Lange-Nielsen syndrome
Romano-Ward syndrome
Short QT syndrome
Neuromyotonia
See also
(20)
Cerebellum
GM2A
Sialidosis
SLC1A3
Autosomal dominant
Autosomal dominant
Autosomal recessive
SCA14
Symptoms
Sca12
Physiologic nystagmus
Dorsal columns
Acetazolamide
Cerebellar vermis
SCA8
Pyruvate dehydrogenase complex
Hyperpnea
Vestibular
NINDS
Parkinsonism
Genetic counselling
more...
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