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Friedreich's Ataxia
Friedreich's ataxia
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Autosomal recessive disorders
Spinal muscular atrophies of childhood
CAMFAK syndrome
Familial isolated vitamin e deficiency
Niemann Pick disease
Fanconi anemia
Neurological disorders
(22)
Cerebellar ataxia
Ataxia
Alpers disease
Acute disseminated encephalomyelitis
Fazio-Londe
Fazio-Londe
Spinocerebellar ataxia
Neurodegenerative disorder
Angelman syndrome
Balo concentric sclerosis
Dysarthria
DRPLA
Fragile x syndrome
Marchiafava Bignami disease
Episodic ataxia
Spinocerebellar ataxia type-6
Machado-joseph disease
Trinucleotide repeat disorders
Multiple sclerosis signs and symptoms
Arachnoiditis
Charcot-Marie Tooth Disease
CAMFAK syndrome
Familial isolated vitamin e deficiency
more...
Genetic disorders
(30)
Ataxia telangiectasia
Female pseudo-Turner syndrome
Myotonic dystrophy
Fibrous dysplasia
Glutaricaciduria
Glutaricaciduria
Faciocutan- eoskeletal syndrome
Spastic ataxia
Acrocephal- opolysyndactyly
Spinal muscular atrophy
Ferrochelatase deficiency
Familial adenomatous polyposis
Spondyloep- imetaphyseal dysplasia, Strudwick type
Fabry disease
Fetal face syndrome
Multiple hereditary exostoses
Fazio-Londe
Spinal muscular atrophies of childhood
CAMFAK syndrome
Spinocerebellar ataxia
Angelman syndrome
DRPLA
Familial isolated vitamin e deficiency
Fragile x syndrome
Episodic ataxia
Spinocerebellar ataxia type-6
Niemann Pick disease
Machado-joseph disease
Trinucleotide repeat disorders
Fanconi anemia
Charcot-Marie Tooth Disease
more...
Diseases and disorders
(58)
Herpesviral encephalitis
Advanced sleep phase syndrome
Demyelinating disease
Amaurosis fugax
Anterior cerebral artery syndrome
Anterior cerebral artery syndrome
Hereditary spinal sclerosis
Dyskinesias
Marburg multiple sclerosis
Gait ataxia
Symptoms
Floating harbor syndrome
Fumarylacetoacetase deficiency disease
Hydrocephalus, normal pressure
Factor V Leiden thrombophilia
Spinocerebellar ataxia 8
Fryns syndrome
Spinocerebellar ataxia 1
Medial pontine syndrome
Craniofrontonasal dysplasia
Lateral pontine syndrome
Aniridia
Multiple system atrophy
Spinocerebellar ataxia 3
Astrocytoma
Dna virus
Alzheimer disease type 2
Amyotrophic lateral sclerosis
Ehlers-danlos syndrome dermatosparaxis type
Neurological disorders
Ataxia
Alpers disease
Acute disseminated encephalomyelitis
Fazio-Londe
Ataxia telangiectasia
Spinal muscular atrophies of childhood
CAMFAK syndrome
Female pseudo-Turner syndrome
Myotonic dystrophy
Fibrous dysplasia
Angelman syndrome
Balo concentric sclerosis
Fragile x syndrome
Glutaricaciduria
Marchiafava Bignami disease
Faciocutan- eoskeletal syndrome
Spastic ataxia
Acrocephal- opolysyndactyly
Spinal muscular atrophy
Niemann Pick disease
Familial adenomatous polyposis
Machado-joseph disease
Spondyloep- imetaphyseal dysplasia, Strudwick type
Fabry disease
Fanconi anemia
Arachnoiditis
Charcot-Marie Tooth Disease
Fetal face syndrome
Multiple hereditary exostoses
more...
Neurology
(16)
The nervous system
Romberg test
Sensory ataxia
Neurological disorders
Acute disseminated encephalomyelitis
Acute disseminated encephalomyelitis
Demyelinating disease
Amaurosis fugax
Dyskinesias
Neurodegenerative disorder
Myotonic dystrophy
Balo concentric sclerosis
Hydrocephalus, normal pressure
Spastic ataxia
Niemann Pick disease
Aniridia
Astrocytoma
more...
Disability
Neurological disorders
Spinocerebellar ataxia
Myotonic dystrophy
Angelman syndrome
Dysarthria
Fragile x syndrome
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...
Motor neuron disease
(11)
ALS Association
ALS Society of Canada
Amyotrophic lateral sclerosis
Monomelic amyotrophy
Motor neurone disease
Motor neurone disease
People with motor neuron disease
Post-polio syndrome
Primary lateral sclerosis
Spinal muscular atrophies of childhood
Spinal muscular atrophy
Split hand syndrome
more...
Nervous system
Leber's hereditary optic neuropathy
Leigh's disease
Neuropathy, ataxia, and retinitis pigmentosa
Lower motor neurone lesion
The nervous system
Symptoms
(16)
Abnormal speech
Diabetes
Dysrhythmias
Hammer toe
Heart disease
Heart disease
Heart failure
Jerky eye movements
Muscle weakness
Pes cavus
Scoliosis
Unsteady gait
Curvature of spine
Ataxia
Amaurosis fugax
Kyphoscoliosis
Inflammatory
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
Frataxin
Systemic atrophies
Congenital malformations
Spinocerebellar
Spinocerebellar
Cerebellum
Idebenone
Dominance (genetics)
Cerebellar diseases
SCA8
Sca12
Kyphoscoliosis
Multiple Sclerosis organizations
Autosomal dominant
Hum. Mol. Genet.
Jean Guyon
Paresthesia
Neurological fatigue
Chromosome 9
Paraneoplastic syndromes
more...
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