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Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

ORPHA:504476DiseaseAutosomal recessiveAdult, Elderly

Ассоциированные гены (1)

RFC1
replication factor C subunit 1
Disease-causing germline mutation(s) in
OMIM: 102579

Фенотипы (16)

Частый (30–79%)16
HP:0000407Sensorineural hearing impairment
HP:0000648Optic atrophy
HP:0000750Delayed speech and language development
HP:0001260Dysarthria
HP:0001284Areflexia
HP:0001310Dysmetria
HP:0002066Gait ataxia
HP:0002073Progressive cerebellar ataxia
HP:0002075Dysdiadochokinesis
HP:0002080Intention tremor
HP:0002460Distal muscle weakness
HP:0002828Multiple joint contractures
HP:0003487Babinski sign
HP:0007108Demyelinating peripheral neuropathy
HP:0007141Sensorimotor neuropathy
HP:0008568Vestibular areflexia

Эпидемиология (2)

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

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы