← Назад

PRKAR1B-related neurodegenerative dementia with intermediate filaments

ORPHA:412066DiseaseAutosomal dominantAdult

Ассоциированные гены (1)

PRKAR1B
protein kinase cAMP-dependent type I regulatory subunit beta
Disease-causing germline mutation(s) in
OMIM: 176911

Фенотипы (23)

Облигатный (100%)1
HP:0000726Dementia
Очень частый (80–99%)5
HP:0000719Inappropriate behavior
HP:0002145Frontotemporal dementia
HP:0002333Motor deterioration
HP:0002354Memory impairment
HP:0012757Abnormal neuron morphology
Частый (30–79%)14
HP:0000736Short attention span
HP:0000739Anxiety
HP:0000741Apathy
HP:0001300Parkinsonism
HP:0002067Bradykinesia
HP:0002172Postural instability
HP:0002362Shuffling gait
HP:0002463Language impairment
HP:0002506Diffuse cerebral atrophy
HP:0002527Falls
HP:0003552Muscle stiffness
HP:0007311Short stepped shuffling gait
HP:0010794Impaired visuospatial constructive cognition
HP:0030216Inertia
Периодический (5–29%)1
HP:0006892Frontotemporal cerebral atrophy
Исключён (0%)2
HP:0002503Spinocerebellar tract degeneration
HP:0007373Motor neuron atrophy

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