Ophtalmological Changes in Prader-Willi Syndrome: Case Report
This work reports a case of Prader-Willi syndrome, with dyschromatopsia, its clinical characteristics and ophthalmological changes, monitoring and treatment, in a 6-year-old child. Prader-Willi syndrome is rare, being an autosomal dominant disorder caused by the exclusion of the proximal long arm of...
| Main Author: | |
|---|---|
| Other Authors: | , , |
| Format: | report |
| Language: | eng |
| Published: |
2022
|
| Subjects: | |
| Online Access: | https://doi.org/10.48560/rspo.25964 |
| Country: | Portugal |
| Oai: | oai:ojs.revistas.rcaap.pt:article/25964 |