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Autosomal recessive spastic paraplegia type 43

ORPHA:320370DiseaseAutosomal recessiveAdolescent, Childhood

Ассоциированные гены (1)

C19ORF12
chromosome 19 open reading frame 12
Disease-causing germline mutation(s) in
OMIM: 614297

Фенотипы (17)

Очень частый (80–99%)7
HP:0001288Gait disturbance
HP:0002064Spastic gait
HP:0002313Spastic paraparesis
HP:0002460Distal muscle weakness
HP:0003487Babinski sign
HP:0003693Distal amyotrophy
HP:0007010Poor fine motor coordination
Частый (30–79%)10
HP:0001257Spasticity
HP:0001290Generalized hypotonia
HP:0001348Brisk reflexes
HP:0001761Pes cavus
HP:0002495Impaired vibratory sensation
HP:0003438Absent Achilles reflex
HP:0006380Knee flexion contracture
HP:0006466Ankle flexion contracture
HP:0007083Hyperactive patellar reflex
HP:0012785Flexion contracture of finger

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