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Machado-Joseph disease type 2

ORPHA:276241Clinical subtypeAutosomal dominantAdult

Ассоциированные гены (1)

ATXN3
ataxin 3
Disease-causing germline mutation(s) in
OMIM: 607047

Фенотипы (34)

Очень частый (80–99%)3
HP:0000590Progressive external ophthalmoplegia
HP:0002071Abnormality of extrapyramidal motor function
HP:0002073Progressive cerebellar ataxia
Частый (30–79%)22
HP:0000520Proptosis
HP:0000623Supranuclear ophthalmoplegia
HP:0000640Gaze-evoked nystagmus
HP:0000651Diplopia
HP:0000750Delayed speech and language development
HP:0001257Spasticity
HP:0001260Dysarthria
HP:0001272Cerebellar atrophy
HP:0001332Dystonia
HP:0001347Hyperreflexia
HP:0002198Dilated fourth ventricle
HP:0002312Clumsiness
HP:0002493Upper motor neuron dysfunction
HP:0002503Spinocerebellar tract degeneration
HP:0003202Skeletal muscle atrophy
HP:0003487Babinski sign
HP:0007089Facial-lingual fasciculations
HP:0007240Progressive gait ataxia
HP:0007256Abnormal pyramidal sign
HP:0009830Peripheral neuropathy
HP:0011960Substantia nigra gliosis
HP:0040140Degeneration of the striatum
Периодический (5–29%)9
HP:0000011Neurogenic bladder
HP:0001605Vocal cord paralysis
HP:0001751Abnormal vestibular function
HP:0002015Dysphagia
HP:0002354Memory impairment
HP:0002360Sleep abnormality
HP:0003394Muscle spasm
HP:0004370Abnormality of temperature regulation
HP:0008944Distal lower limb amyotrophy

Эпидемиология (1)

Point prevalence
Unknown
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы