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Progressive multifocal leukoencephalopathy

ORPHA:217260DiseaseNot applicableAll ages

Фенотипы (35)

Очень частый (80–99%)8
HP:0000707Abnormality of the nervous system
HP:0002721Immunodeficiency
HP:0002921Abnormality of the cerebrospinal fluid
HP:0004302Functional motor deficit
HP:0007305CNS demyelination
HP:0031392Abnormal proportion of CD4 T cells
HP:0100706Abnormality of the oligodendroglia
HP:0100707Abnormal astrocyte morphology
Частый (30–79%)12
HP:0000505Visual impairment
HP:0001260Dysarthria
HP:0001268Mental deterioration
HP:0002066Gait ataxia
HP:0002167Abnormality of speech or vocalization
HP:0002315Headache
HP:0003474Somatic sensory dysfunction
HP:0003690Limb muscle weakness
HP:0004374Hemiplegia/hemiparesis
HP:0005415Decreased proportion of CD8-positive T cells
HP:0010549Weakness due to upper motor neuron dysfunction
HP:0100543Cognitive impairment
Периодический (5–29%)11
HP:0000639Nystagmus
HP:0000751Personality changes
HP:0001123Visual field defect
HP:0001250Seizure
HP:0001300Parkinsonism
HP:0002321Vertigo
HP:0002381Aphasia
HP:0004377Hematological neoplasm
HP:0012246Oculomotor nerve palsy
HP:0025479Self-neglect
HP:0030516Homonymous hemianopia
Очень редкий (1–4%)4
HP:0000651Diplopia
HP:0001287Meningitis
HP:0001310Dysmetria
HP:0003401Paresthesia

Эпидемиология (3)

Point prevalence
Unknown
Worldwide
Annual incidence
<1 / 1 000 000
Sweden
Annual incidence
1-9 / 1 000 000
France

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы