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MT-ATP6-related mitochondrial spastic paraplegia

ORPHA:320360DiseaseMitochondrial inheritanceAdult

Ассоциированные гены (1)

MT-ATP6
mitochondrially encoded ATP synthase membrane subunit 6
Disease-causing germline mutation(s) in
OMIM: 516060

Фенотипы (17)

Очень частый (80–99%)3
HP:0002166Impaired vibration sensation in the lower limbs
HP:0007020Progressive spastic paraplegia
HP:0012514Lower limb pain
Частый (30–79%)5
HP:0001288Gait disturbance
HP:0001347Hyperreflexia
HP:0002061Lower limb spasticity
HP:0003477Peripheral axonal neuropathy
HP:0009053Distal lower limb muscle weakness
Периодический (5–29%)7
HP:0000819Diabetes mellitus
HP:0001317Abnormal cerebellum morphology
HP:0001638Cardiomyopathy
HP:0003487Babinski sign
HP:0005115Supraventricular arrhythmia
HP:0007256Abnormal pyramidal sign
HP:0008969Leg muscle stiffness
Исключён (0%)2
HP:0000648Optic atrophy
HP:0002151Increased circulating lactate concentration

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