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Autosomal recessive spastic paraplegia type 69

ORPHA:401830DiseaseAutosomal recessiveInfancy

Ассоциированные гены (1)

RAB3GAP2
RAB3 GTPase activating non-catalytic protein subunit 2
Disease-causing germline mutation(s) in
OMIM: 609275

Фенотипы (13)

Частый (30–79%)13
HP:0000365Hearing impairment
HP:0000518Cataract
HP:0001256Intellectual disability, mild
HP:0001263Global developmental delay
HP:0001274Agenesis of corpus callosum
HP:0002061Lower limb spasticity
HP:0002120Cerebral cortical atrophy
HP:0002378Hand tremor
HP:0002464Spastic dysarthria
HP:0006817Aplasia/Hypoplasia of the cerebellar vermis
HP:0007020Progressive spastic paraplegia
HP:0012447Abnormal myelination
HP:0100022Abnormality of movement

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