Michels syndrome is a syndrome characterised by intellectual disability, craniosynostosis, blepharophimosis, ptosis, epicanthus inversus,[2][3] highly arched eyebrows, and hypertelorism.[3][4] 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.[3][4]
| Michels syndrome | |
|---|---|
| Other names | Oculopalatoskeletal syndrome |
 | |
| This condition is inherited in an autosomal recessive manner[1] | |
| Specialty | Medical genetics |
See also
- Malpuech facial clefting syndrome, another condition in the 3MC spectrum