Conditions / Syndrome
Sotos syndrome 2
info · Syndrome
A Sotos syndrome that has_material_basis_in heterozygous mutation in the NFIX gene on chromosome 19p13.
Signs and symptoms
- Anxiety
- Overgrowth
- Macrocephaly
- Intellectual disability
- Delayed speech and language development
- High forehead
- Hypotonia
- Narrow face
- Downslanted palpebral fissures
- Long face
Also known as: SOTOS2