Michels syndrome

Michels syndrome
Other namesOculopalatoskeletal syndrome
This condition is inherited in an autosomal recessive manner
SpecialtyMedical genetics

Michels syndrome is a syndrome characterised by intellectual disability, craniosynostosis, blepharophimosis, ptosis, epicanthus inversus, highly arched eyebrows, and hypertelorism. People with Michels syndrome vary in other symptoms such as asymmetry of the skull, eyelid, and anterior chamber anomalies, cleft lip and palate, umbilical anomalies, and growth and cognitive development.