vitalwiki

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