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15q11q13 microduplication syndrome

ORPHA:238446Malformation syndromeNot applicable, UnknownInfancy, Neonatal

Ассоциированные гены (1)

UBE3A
ubiquitin protein ligase E3A
Role in the phenotype of
OMIM: 601623

Фенотипы (19)

Очень частый (80–99%)6
HP:0000722Compulsive behaviors
HP:0000750Delayed speech and language development
HP:0001249Intellectual disability
HP:0001252Hypotonia
HP:0001263Global developmental delay
HP:0007018Attention deficit hyperactivity disorder
Частый (30–79%)4
HP:0000717Autism
HP:0001250Seizure
HP:0002186Apraxia
HP:0004209Clinodactyly of the 5th finger
Периодический (5–29%)9
HP:0000256Macrocephaly
HP:0000286Epicanthus
HP:0000298Mask-like facies
HP:0000494Downslanted palpebral fissures
HP:0001251Ataxia
HP:0001382Joint hypermobility
HP:0004322Short stature
HP:0006101Finger syndactyly
HP:0030680Abnormal cardiovascular system morphology

Эпидемиология (2)

Point prevalence
<1 / 1 000 000
Worldwide
Cases/families
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы