Abstract
We report on a 2-year-old girl with Michels syndrome, a condition characterized by mental deficiency, craniosynostosis, blepharophimosis, ptosis, and epicanthus inversus. The phenotypic findings are compared with those of previously reported cases.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 28-30 |
| Number of pages | 3 |
| Journal | American journal of medical genetics |
| Volume | 37 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1990 |
Keywords
- Michels syndrome
- autosomal recessive inheritance
- craniosynostosis
- lid abnormalities
ASJC Scopus subject areas
- Genetics(clinical)