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ANK3-related intellectual disability-sleep disturbance syndrome

ORPHA:356996DiseaseAutosomal recessiveChildhood

Ассоциированные гены (1)

ANK3
ankyrin 3
Disease-causing germline mutation(s) in
OMIM: 600465

Фенотипы (13)

Частый (30–79%)9
HP:0000718Aggressive behavior
HP:0000729Autistic behavior
HP:0000750Delayed speech and language development
HP:0000752Hyperactivity
HP:0001252Hypotonia
HP:0001257Spasticity
HP:0002342Intellectual disability, moderate
HP:0002360Sleep abnormality
HP:0003763Bruxism
Периодический (5–29%)4
HP:0000256Macrocephaly
HP:0001250Seizure
HP:0001256Intellectual disability, mild
HP:0001520Large for gestational age

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