Conditions / Syndrome
Crouzon syndrome-acanthosis nigricans syndrome
info · Syndrome
A syndrome characterized by Crouzon-like features, premature synostosis of cranial sutures, and acanthosis nigricans that has_material_basis_in heterozygous missense mutation in the FGFR3 gene on chromosome 4p16.
Signs and symptoms
- Midface retrusion
- Acanthosis nigricans
- Proptosis
- Hydrocephalus
- Craniosynostosis
- Choanal atresia
- Hypertelorism
- Brachycephaly
- Melanocytic nevus
Also known as: CAN; Crouzon-dermoskeletal syndrome; Crouzonodermoskeletal syndrome