Intelligenzminderung durch Punktmutationen im DYRK1A-Gen
ORPHA:464311· ICD-10 Q87.8· Intellectual disability syndrome due to a DYRK1A point mutation
- Prävalenz
- <1 / 1 000 000
- Vererbung
- Autosomal dominant
- Erkrankungsalter
- Infancy, Neonatal
ORPHA:464311· ICD-10 Q87.8· Intellectual disability syndrome due to a DYRK1A point mutation