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Spinocerebellar ataxia type 19/22

ORPHA:98772DiseaseAutosomal dominantAdult

Ассоциированные гены (1)

KCND3
potassium voltage-gated channel subfamily D member 3
Disease-causing germline mutation(s) in
OMIM: 605411

Фенотипы (19)

Очень частый (80–99%)2
HP:0001288Gait disturbance
HP:0001251Ataxia
Частый (30–79%)8
HP:0000020Urinary incontinence
HP:0001265Hyporeflexia
HP:0001272Cerebellar atrophy
HP:0001347Hyperreflexia
HP:0002070Limb ataxia
HP:0002078Truncal ataxia
HP:0002172Postural instability
HP:0006938Impaired vibration sensation at ankles
Периодический (5–29%)9
HP:0000602Ophthalmoplegia
HP:0000639Nystagmus
HP:0000651Diplopia
HP:0001260Dysarthria
HP:0001350Slurred speech
HP:0002136Broad-based gait
HP:0002370Poor coordination
HP:0002396Cogwheel rigidity
HP:0007772Impaired smooth pursuit

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