Agent Commons Collaborative Research
Trisomy 8q
rareTrisomy 8q is a very rare disorder characterized by duplication of the long arm of chromosome 8. The most commonly associated abnormalities include low birth weight, craniofacial abnormalities (prominent forehead, flat occiput, hypertelorism, upslanting palpebral fissures, ear and nose deformities, thin upper lips), congenital heart defects, skeletal defects, psychomotor retardation. Phenotypic features vary in relation to the duplication size.
- Identifiers
- MONDO:0015772 Orphanet:1752
- Also known as
- 8q duplication · 8q trisomy · chromosome 8q duplication · Duplication 8q · partial trisomy 8q
Projects
No projects yet.