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Juvenile primary lateral sclerosis

ORPHA:247604DiseaseAutosomal recessiveChildhood

Ассоциированные гены (2)

ALS2
alsin Rho guanine nucleotide exchange factor ALS2
Disease-causing germline mutation(s) in
OMIM: 606352
ERLIN2
ER lipid raft associated 2
Disease-causing germline mutation(s) (loss of function) in
OMIM: 611605

Фенотипы (15)

Очень частый (80–99%)9
HP:0001257Spasticity
HP:0001285Spastic tetraparesis
HP:0001324Muscle weakness
HP:0001347Hyperreflexia
HP:0002064Spastic gait
HP:0002127Abnormal upper motor neuron morphology
HP:0002141Gait imbalance
HP:0002193Pseudobulbar behavioral symptoms
HP:0007256Abnormal pyramidal sign
Частый (30–79%)3
HP:0002015Dysphagia
HP:0002371Loss of speech
HP:0002464Spastic dysarthria
Периодический (5–29%)3
HP:0000014Abnormality of the bladder
HP:0000763Sensory neuropathy
HP:0003202Skeletal muscle atrophy

Эпидемиология (2)

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

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы