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Spinocerebellar ataxia type 43

ORPHA:497764DiseaseAutosomal dominantAdult, Elderly

Ассоциированные гены (1)

MME
membrane metalloendopeptidase
Disease-causing germline mutation(s) in
OMIM: 120520

Фенотипы (22)

Очень частый (80–99%)3
HP:0003477Peripheral axonal neuropathy
HP:0008959Distal upper limb muscle weakness
HP:0009053Distal lower limb muscle weakness
Частый (30–79%)16
HP:0000571Hypometric saccades
HP:0000768Pectus carinatum
HP:0001260Dysarthria
HP:0001265Hyporeflexia
HP:0001284Areflexia
HP:0001761Pes cavus
HP:0002066Gait ataxia
HP:0002070Limb ataxia
HP:0002317Unsteady gait
HP:0002396Cogwheel rigidity
HP:0002936Distal sensory impairment
HP:0003387Decreased number of large peripheral myelinated nerve fibers
HP:0003693Distal amyotrophy
HP:0007141Sensorimotor neuropathy
HP:0009027Foot dorsiflexor weakness
HP:0012531Pain
Периодический (5–29%)2
HP:0002073Progressive cerebellar ataxia
HP:0006855Cerebellar vermis atrophy
Исключён (0%)1
HP:0000726Dementia

Эпидемиология (2)

Cases/families
Worldwide
Point prevalence
<1 / 1 000 000
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы