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Episodic ataxia type 1

ORPHA:37612DiseaseAutosomal dominantAdolescent, Childhood

Ассоциированные гены (1)

KCNA1
potassium voltage-gated channel subfamily A member 1
Disease-causing germline mutation(s) in
OMIM: 176260

Фенотипы (27)

Очень частый (80–99%)3
HP:0002172Postural instability
HP:0002370Poor coordination
HP:0002411Myokymia
Частый (30–79%)10
HP:0000622Blurred vision
HP:0000651Diplopia
HP:0000975Hyperhidrosis
HP:0001260Dysarthria
HP:0002018Nausea
HP:0002312Clumsiness
HP:0002315Headache
HP:0002321Vertigo
HP:0003394Muscle spasm
HP:0003552Muscle stiffness
Периодический (5–29%)14
HP:0000750Delayed speech and language development
HP:0001188Hand clenching
HP:0001266Choreoathetosis
HP:0001270Motor delay
HP:0001272Cerebellar atrophy
HP:0001276Hypertonia
HP:0001328Specific learning disability
HP:0002098Respiratory distress
HP:0002486Myotonia
HP:0002650Scoliosis
HP:0002751Kyphoscoliosis
HP:0005461Craniofacial disproportion
HP:0008981Calf muscle hypertrophy
HP:0030051Tip-toe gait

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