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Autosomal dominant spastic paraplegia type 9B

ORPHA:447757DiseaseAutosomal dominantAdolescent, Adult, Infancy

Ассоциированные гены (1)

ALDH18A1
aldehyde dehydrogenase 18 family member A1
Disease-causing germline mutation(s) (loss of function) in
OMIM: 138250

Фенотипы (21)

Частый (30–79%)12
HP:0001761Pes cavus
HP:0002064Spastic gait
HP:0002174Postural tremor
HP:0002344Progressive neurologic deterioration
HP:0002464Spastic dysarthria
HP:0002493Upper motor neuron dysfunction
HP:0002505Loss of ambulation
HP:0003487Babinski sign
HP:0007083Hyperactive patellar reflex
HP:0007178Motor polyneuropathy
HP:0007240Progressive gait ataxia
HP:0007350Hyperreflexia in upper limbs
Периодический (5–29%)9
HP:0000519Developmental cataract
HP:0000726Dementia
HP:0001252Hypotonia
HP:0002020Gastroesophageal reflux
HP:0002987Elbow flexion contracture
HP:0003438Absent Achilles reflex
HP:0003477Peripheral axonal neuropathy
HP:0004373Focal dystonia
HP:0006827Atrophy of the spinal cord

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