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Hereditary Spastic Paraplegia
Hereditary spastic paraplegia
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Neurology
(14)
Demyelinating disease
Acute disseminated encephalomyelitis
Amaurosis fugax
Hydrocephalus, normal pressure
Balo concentric sclerosis
Balo concentric sclerosis
Central nervous system
Myoclonic Encephalopathy of infants
Adrenoleuk- odystrophy
J. Neurol.
Ramsay Hunt syndrome type I
Neuropathies
Acquired epileptiform aphasia
Dystonia
Neurological examination
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Genetic disorders
(13)
Fazio-Londe
CAMFAK syndrome
Spinal muscular atrophies of childhood
Charcot-Marie Tooth Disease
Glutaricaciduria
Glutaricaciduria
Mulibrey nanism
VATER syndrome
Popliteal pterygium syndrome
HMSN
Otospondyl- omegaepiphyseal dysplasia
Fabry disease
Meckel-Gruber syndrome
Adrenoleuk- odystrophy
more...
Diseases and disorders
(48)
Alpers disease
Herpesviral encephalitis
Advanced sleep phase syndrome
Spastic paraparesis
Henoch–Schönlein purpura
Henoch–Schönlein purpura
Anterior cerebral artery syndrome
Marburg multiple sclerosis
Primary lateral sclerosis
Marchiafava Bignami disease
Craniofrontonasal dysplasia
Polyglucosan body disease adult
Paraplegia
Floating harbor syndrome
X-linked hypophosphatemic rickets
Spinocerebellar ataxia 7
Progressive supranuclear palsy
Hydrolethalus syndrome
Dna virus
Amyotrophic lateral sclerosis
Rna virus
Haim-munk syndrome
Hemiplegia
Refsum disease
Optic atrophies, hereditary
Hereditary angioedema
Opitz syndrome
Factor V Leiden thrombophilia
Blepharophimosis ptosis epicanthus inversus
Progressive bulbar palsy
Tropical spastic paraparesis
Motor neurone disease
Myelopathy
Demyelinating disease
Fazio-Londe
CAMFAK syndrome
Acute disseminated encephalomyelitis
Spinal muscular atrophies of childhood
Amaurosis fugax
Charcot-Marie Tooth Disease
Glutaricaciduria
Hydrocephalus, normal pressure
Balo concentric sclerosis
Neuropathies
VATER syndrome
Popliteal pterygium syndrome
HMSN
Dystonia
Fabry disease
more...
Neurological disorders
(12)
Multiple sclerosis signs and symptoms
Alpers disease
Fazio-Londe
CAMFAK syndrome
Acute disseminated encephalomyelitis
Acute disseminated encephalomyelitis
Charcot-Marie Tooth Disease
Marchiafava Bignami disease
Balo concentric sclerosis
Neuropathies
HMSN
Meckel-Gruber syndrome
Motor neurone disease
more...
Rare diseases
CAMFAK syndrome
Mulibrey nanism
Amyotrophic lateral sclerosis
Popliteal pterygium syndrome
Fabry disease
Meckel-Gruber syndrome
Motor neurone disease
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)
Hirayama syndrome
ALS Association
ALS Society of Canada
Amyotrophic lateral sclerosis
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...
Extrapyramidal and movement disorders
(19)
Hallervorden-spatz syndrome
Postencephalitic parkinsonism
Akathisia
Blepharospasm
Choreia (disease)
Choreia (disease)
Dystonia
Essential tremor
Meige's syndrome
Movement disorder
Multiple system atrophy
Myoclonus
Neuroleptic malignant syndrome
Parkinson's disease
Parkinsonism
Progressive supranuclear palsy
Restless legs syndrome
Spasmodic torticollis
Stiff person syndrome
Tardive dyskinesia
more...
Gene
(9)
NIPA1
SPG3A
SPG7
SPG20
SPG11
SPG11
KIF5A
Spastin
REEP1
ALS2
more...
Flaccid paralysis
Spastic paraplegia
Lower motor neuron lesion
Spastic diplegia
Upper motor neuron lesion
Motor neurone disease
(10)
Infantile progressive bulbar palsy
Kennedy's disease
Lower motor neuron
Progressive muscular atrophy
Pseudobulbar palsy
Pseudobulbar palsy
Upper motor neuron
X-linked spinal muscular atrophy 2
Survival motor neuron spinal muscular atrophy
Primary lateral sclerosis
Spinal muscular atrophy
more...
See also
(20)
Systemic atrophies
Spastin
Spasticity
Congenital malformations
Autosomal dominant
Autosomal dominant
Autosomal recessive
REEP1
Increased muscle tone
Spastic
Bulbar
Nervous system
Motor neuron
Ann. Neurol.
Multiple Sclerosis organizations
Neurological fatigue
Fanconi
Axonal
ICHD-2
Hereditary
Friedreich
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