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Friedreich Ataxia
Friedreich ataxia
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Autosomal recessive disorders
(10)
Spinal muscular atrophies of childhood
CAMFAK syndrome
Familial isolated vitamin e deficiency
Familial dysautonomia
Amylo-1,6-- glucosidase deficiency
Amylo-1,6-- glucosidase deficiency
Ataxia with Lactic Acidosis, Type II
Abetalipop- roteinemia
ACADM deficiency
Familial mediterranean fever
Shwachman syndrome
more...
Neurological disorders
(21)
Acute disseminated encephalomyelitis
Fazio-Londe
Spinocerebellar ataxia
Marchiafava Bignami disease
Foix-Alajouanine syndrome
Foix-Alajouanine syndrome
Cerebellar ataxia
Alpers disease
Hemiballismus
Olivoponto- cerebellar atrophy
Episodic ataxia
Kennedy disease
Trinucleotide repeat
Dysarthria
Aicardi syndrome
Neurodegenerative disorder
Multiple sclerosis signs and symptoms
Balo concentric sclerosis
SCA6
CAMFAK syndrome
Familial isolated vitamin e deficiency
Familial dysautonomia
more...
Genetic disorders
(30)
Ataxia telangiectasia
Mitochondrial diseases
Female pseudo-Turner syndrome
Alexander disease
Glutaricaciduria
Glutaricaciduria
Myotonic dystrophy
Anderson-Warburg syndrome
HPRT - Hypoxanthi- ne-guanine phosphorib- osyltransferase deficiency
Acral dysostosis with facial and genital abnormalities
VATER syndrome
Spondylometaphyseal Dysplasia, Strudwick Type
Pallister-Hall syndrome
Multiple hereditary exostoses
Thrombocytopenia absent radius
Fazio-Londe
Spinal muscular atrophies of childhood
CAMFAK syndrome
Spinocerebellar ataxia
Episodic ataxia
Kennedy disease
Familial isolated vitamin e deficiency
Trinucleotide repeat
Amylo-1,6-- glucosidase deficiency
Ataxia with Lactic Acidosis, Type II
Abetalipop- roteinemia
Aicardi syndrome
ACADM deficiency
Familial mediterranean fever
Shwachman syndrome
SCA6
more...
Diseases and disorders
(59)
Advanced sleep phase syndrome
Herpesviral encephalitis
Hydrocephalus, normal pressure
Striatonigral degeneration
Basal ganglia disease
Basal ganglia disease
Herpesviral
Syringobulbia
Spinocerebellar ataxia 8
Anterior cerebral artery syndrome
Symptoms
Floating harbor syndrome
Hereditary spinal sclerosis
Narcolepsy- -Cataplexy
Amaurosis fugax
Spinocerebellar ataxia 1
Fumarylacetoacetase deficiency disease
Episodic ataxia syndrome
Craniofrontonasal dysplasia
Aniridia cerebellar ataxia mental deficiency
Acidemia isovaleric
Marburg multiple sclerosis
Gait ataxia
Opitz syndrome
Factor V Leiden thrombophilia
Dyskinesias
Dysdiadochokinesia
Central pontine myelinolysis
Fryns syndrome
Alpha-neuraminidase deficiency
Androgen insensitivity syndrome partial
Acute disseminated encephalomyelitis
Fazio-Londe
Spinal muscular atrophies of childhood
CAMFAK syndrome
Marchiafava Bignami disease
Foix-Alajouanine syndrome
Alpers disease
Ataxia telangiectasia
Olivoponto- cerebellar atrophy
Mitochondrial diseases
Female pseudo-Turner syndrome
Alexander disease
Kennedy disease
Glutaricaciduria
Familial dysautonomia
Myotonic dystrophy
Anderson-Warburg syndrome
HPRT - Hypoxanthi- ne-guanine phosphorib- osyltransferase deficiency
Ataxia with Lactic Acidosis, Type II
Abetalipop- roteinemia
Acral dysostosis with facial and genital abnormalities
VATER syndrome
Spondylometaphyseal Dysplasia, Strudwick Type
Familial mediterranean fever
Balo concentric sclerosis
Pallister-Hall syndrome
Multiple hereditary exostoses
Thrombocytopenia absent radius
Shwachman syndrome
more...
Sleep disorders
Delayed sleep phase
Advanced sleep phase syndrome
Narcolepsy- -Cataplexy
Syndromes
(8)
Paraneoplastic syndromes
Advanced sleep phase syndrome
CAMFAK syndrome
Delayed sleep phase
Female pseudo-Turner syndrome
Female pseudo-Turner syndrome
Familial dysautonomia
HPRT - Hypoxanthi- ne-guanine phosphorib- osyltransferase deficiency
Acral dysostosis with facial and genital abnormalities
more...
Multiple sclerosis
(24)
Acute disseminated encephalomyelitis
Balo concentric sclerosis
Calcium 2-aminoeth- ylphosphate
Clinically isolated syndrome
Corinne Goldsmith Dickinson Center for Multiple Sclerosis
Corinne Goldsmith Dickinson Center for Multiple Sclerosis
Diffuse myelinoclastic sclerosis
Dirucotide
Expanded Disability Status Scale
Idiopathic inflammatory demyelinating diseases
Low dose naltrexone
Marburg multiple sclerosis
McDonald criteria
Multiple Sclerosis International Federation
Multiple sclerosis organizations
Multiple sclerosis signs and symptoms
Neuromyelitis optica
Pathophysiology of multiple sclerosis
People with multiple sclerosis
Poser criteria
Swank diet
Therapies under investigation for multiple sclerosis
Transverse myelitis
Treatment of multiple sclerosis
Uhthoff's phenomenon
more...
Medicine
Vascular myelopathy
Intracranial hypotension
Kyphoscoliosis
Diseases and disorders
Gene
Frataxin
SCA16
PLEKHG4
Sca12
ATXN10
SCA14
Symptoms
(16)
Unsteady gait
Abnormal speech
Ataxia
Diabetes
Dysrhythmias
Dysrhythmias
Hammer toe
Heart disease
Heart failure
Jerky eye movements
Muscle weakness
Pes cavus
Scoliosis
Amaurosis fugax
Kyphoscoliosis
Spastic paralysis
Dysdiadochokinesia
more...
Signs and tests
(9)
CT
EMG
Electrocardiography
MRI of the head
Muscle biopsy
Muscle biopsy
Nerve conduction tests
X-ray
X-ray of the chest
X-ray of the spine
more...
See also
(20)
Friedreich
Systemic atrophies
Postencephalitic parkinsonism
Pantothenate kinase-associated neurodegeneration
Idebenone
Idebenone
Spinocerebellar
Deferiprone
Cerebellar diseases
Cerebellum
Spinal cord diseases
Lacunar stroke
Foot deformities
Agnosia, primary visual
Vitamin e deficiency
Chromosome 9
Dominance (genetics)
Riluzole
Corticospinal
Spastic paralysis
Walking style
more...
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