Apert syndrome: A rare case requiring multidisciplinary approach for a better living
A 7-year-old boy presented with watering, prominent eyes and defective vision. He had brachycephaly, hypertelorism, shallow proptotic orbits, large exotropia, and syndactyly of the hands and feet. Lateral cephalogram showed fused sutures and mid-facial hypoplasia. He had typical features and diagnos...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2021-01-01
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| Series: | TNOA Journal of Ophthalmic Science and Research |
| Subjects: | |
| Online Access: | http://www.tnoajosr.com/article.asp?issn=2589-4528;year=2021;volume=59;issue=1;spage=91;epage=94;aulast=Elizabeth |