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Expanding the Spectrum of Oculocutaneous Albinism: Does Isolated Foveal Hypoplasia Really Exist?
Oculocutaneous albinism is an autosomal recessive disorder characterized by the presence of typical ocular features, such as foveal hypoplasia, iris translucency, hypopigmented fundus oculi and reduced pigmentation of skin and hair. Albino patients can show significant clinical variability; some ind...
Autores principales: | Rocca, Camilla, Tiberi, Lucia, Bargiacchi, Sara, Palazzo, Viviana, Landini, Samuela, Marziali, Elisa, Caputo, Roberto, Tinelli, Francesca, Marchi, Viviana, Benedetto, Alessandro, Pagliazzi, Angelica, Bacci, Giacomo Maria |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9317384/ https://www.ncbi.nlm.nih.gov/pubmed/35887175 http://dx.doi.org/10.3390/ijms23147825 |
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