A disorder caused by loss of maternal UBE3A function through a 15q11-q13 deletion, paternal uniparental disomy, an imprinting defect or a UBE3A variant.
Mit változtat a diagnózis
Seizure, sleep and developmental support; families with a maternally inherited UBE3A variant have a 50% recurrence risk, so genetic counselling is important.
Vizsgált gének
Más néven
Angelman syndrome (Type 1); Angelman syndrome (Type 2); Angelman’s syndrome; AS; happy puppet syndrome (formerly)
4 kapcsolódó altípust tartalmaz ↓Altípusok elrejtése ↑
- Angelman syndrome due to a point mutation
- Angelman syndrome due to imprinting defect in 15q11-q13
- Angelman syndrome due to maternal 15q11q13 deletion
- Angelman syndrome due to paternal uniparental disomy of chromosome 15
