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Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome

ORPHA:263410DiseaseAutosomal recessiveInfancy, Neonatal

Ассоциированные гены (1)

SLC19A3
solute carrier family 19 member 3
Disease-causing germline mutation(s) in
OMIM: 606152

Фенотипы (25)

Очень частый (80–99%)3
HP:0001263Global developmental delay
HP:0002134Abnormality of the basal ganglia
HP:0012697Small basal ganglia
Частый (30–79%)15
HP:0000711Restlessness
HP:0000737Irritability
HP:0001250Seizure
HP:0001251Ataxia
HP:0001260Dysarthria
HP:0001289Confusion
HP:0001332Dystonia
HP:0001347Hyperreflexia
HP:0002273Tetraparesis
HP:0002329Drowsiness
HP:0002465Poor speech
HP:0007105Infantile encephalopathy
HP:0007185Loss of consciousness
HP:0012747Abnormal brainstem MRI signal intensity
HP:0030215Inappropriate crying
Периодический (5–29%)7
HP:0000494Downslanted palpebral fissures
HP:0002093Respiratory insufficiency
HP:0002133Status epilepticus
HP:0002510Spastic tetraplegia
HP:0004302Functional motor deficit
HP:0008947Floppy infant
HP:0012469Infantile spasms

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