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Intellectual disability-hyperkinetic movement-truncal ataxia syndrome

ORPHA:369847DiseaseAutosomal recessiveChildhood

Ассоциированные гены (1)

TRAPPC11
trafficking protein particle complex subunit 11
Disease-causing germline mutation(s) in
OMIM: 614138

Фенотипы (20)

Частый (30–79%)13
HP:0000518Cataract
HP:0001249Intellectual disability
HP:0001263Global developmental delay
HP:0001288Gait disturbance
HP:0002072Chorea
HP:0002078Truncal ataxia
HP:0002487Hyperkinetic movements
HP:0002650Scoliosis
HP:0003198Myopathy
HP:0003326Myalgia
HP:0006785Limb-girdle muscular dystrophy
HP:0009020Exercise-induced muscle fatigue
HP:0009073Progressive proximal muscle weakness
Периодический (5–29%)7
HP:0000486Strabismus
HP:0000545Myopia
HP:0001250Seizure
HP:0002059Cerebral atrophy
HP:0002091Restrictive ventilatory defect
HP:0005133Right ventricular dilatation
HP:0008947Floppy infant

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