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Mitochondrial membrane protein-associated neurodegeneration

ORPHA:289560DiseaseAutosomal recessiveAdolescent, Adult, Childhood

Ассоциированные гены (1)

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

Фенотипы (26)

Очень частый (80–99%)9
HP:0000708Atypical behavior
HP:0001257Spasticity
HP:0001260Dysarthria
HP:0001268Mental deterioration
HP:0001324Muscle weakness
HP:0002063Rigidity
HP:0002172Postural instability
HP:0002378Hand tremor
HP:0003487Babinski sign
Частый (30–79%)14
HP:0000020Urinary incontinence
HP:0000648Optic atrophy
HP:0001288Gait disturbance
HP:0001300Parkinsonism
HP:0001332Dystonia
HP:0002015Dysphagia
HP:0002067Bradykinesia
HP:0002313Spastic paraparesis
HP:0002359Frequent falls
HP:0002453Abnormal globus pallidus morphology
HP:0002607Bowel incontinence
HP:0006801Hyperactive deep tendon reflexes
HP:0007002Motor axonal neuropathy
HP:0045007Abnormality of the substantia nigra
Периодический (5–29%)2
HP:0000570Abnormal saccadic eye movements
HP:0002362Shuffling gait
Очень редкий (1–4%)1
HP:0002093Respiratory insufficiency

Эпидемиология (1)

Point prevalence
1-9 / 1 000 000
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы