Craniorhiny is a rare autosomal dominant syndrome characterized by craniosynostosis (oxycephaly) and facial anomalies around the nose base and lips.
Signs and symptoms
Features of this condition include: • Head or neck: anteverted nares, wide nose, recessed forehead • Integument: nasal hirsutism • Musculoskeletal system: craniosynotosis, oxycephaly/turricephaly Infranasal spherical cyst-like formations with fistulas have also been seen. == History ==
History
The first (and only confirmed) reports of this condition was made in 1991, seen in a father and son. Two siblings reported in 2007 are also speculated to have the condition. ==References==