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...
| Autor principal: | |
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| Outros Autores: | , , |
| Formato: | report |
| Idioma: | eng |
| Publicado em: |
2022
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| Assuntos: | |
| Texto completo: | https://doi.org/10.48560/rspo.25964 |
| País: | Portugal |
| Oai: | oai:ojs.revistas.rcaap.pt:article/25964 |