Conditions / Syndrome
Seckel syndrome 9
info · Syndrome
A Seckel syndrome that has_material_basis_in homozygous mutation in the TRAIP gene on chromosome 3p21.
Signs and symptoms
- Short stature
- Protruding ear
- Narrow face
- Microcephaly
- Long face
- Global developmental delay
- Intrauterine growth retardation
- Micrognathia
- Scaphocephaly
- Dolichocephaly
Also known as: SCKL9