Синдром мікроделеції 8q21.11
ORPHA:284160· ICD-10 Q93.5· 8q21.11 microdeletion syndrome
Визначення(English summary)
8q21.11 microdeletion syndrome encompasses heterozygous overlapping microdeletions on chromosome 8q21.11 resulting in intellectual disability, facial dysmorphism comprising a round face, ptosis, short philtrum, Cupid's bow and prominent low-set ears, nasal speech and mild finger and toe anomalies.
- Поширеність
- <1 / 1 000 000
- Успадкування
- Autosomal dominant, Not applicable
- Вік початку
- Infancy, Neonatal