SE-ATLAS

Syndrome de Foix-Chavany-Marie Syndrome de paralysie supranucléaire progressive-akinésie pure avec freezing de la marche Syndrome corticobasal Syndrome de paralysie supranucléaire progressive-syndrome corticobasal Syndrome de Dubowitz Syndrome de Leigh Neuropathie motrice distale héréditaire type 2 Paralysie spastique infantile ascendante héréditaire Syndrome de Cockayne Syndrome de paralysie supranucléaire progressive classique Neuropathie motrice distale héréditaire type 1 Atrophie musculaire progressive Atrophie multisystématisée type cérébelleux Neuropathie motrice distale héréditaire type 5 Syndrome de paralysie supranucléaire progressive-parkinsonisme Maladie des inclusions intranucléaires neuronales Dystrophie neuroaxonale infantile Neuropathie motrice distale héréditaire type Jerash Neuropathie motrice distale héréditaire type 7 Huntington disease Motor neuron disease Frontotemporal degeneration with dementia MELAS Susac syndrome Amyotrophic lateral sclerosis type 4 Kennedy disease Progressive supranuclear palsy-progressive non-fluent aphasia syndrome Noonan syndrome Aarskog-Scott syndrome Subacute sclerosing leukoencephalitis Moyamoya disease Seckel syndrome Progressive supranuclear palsy Amyotrophic lateral sclerosis Robinow syndrome Multiple system atrophy, parkinsonian type Madras motor neuron disease Logopenic progressive aphasia ITM2B amyloidosis Smith-Lemli-Opitz syndrome Frontotemporal dementia, right temporal atrophy variant Primary lateral sclerosis Young adult-onset distal hereditary motor neuropathy Spinal atrophy-ophthalmoplegia-pyramidal syndrome Moyamoya disease with early-onset achalasia X-linked distal hereditary motor neuropathy HERNS syndrome Watson syndrome Primary angiitis of the central nervous system Primary progressive aphasia Semantic dementia Autosomal recessive lower motor neuron disease with childhood onset Neuromyelitis optica spectrum disorder 17q11 microdeletion syndrome Autosomal recessive distal hereditary motor neuropathy Monosomy 22q13.3 Atypical progressive supranuclear palsy syndrome Juvenile primary lateral sclerosis Juvenile amyotrophic lateral sclerosis Sporadic infantile bilateral striatal necrosis Behavioral variant of frontotemporal dementia Progressive non-fluent aphasia Parkinson-dementia complex of Guam Infectious encephalitis Reversible cerebral vasoconstriction syndrome Familial cerebral saccular aneurysm Cerebral sinovenous thrombosis Infantile bilateral striatal necrosis Familial infantile bilateral striatal necrosis Frontotemporal dementia Legius syndrome Hereditary spastic paraplegia Posterior cortical atrophy Encephalitis Neurofibromatosis type 1 Full NF2-related schwannomatosis