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Griscelli Syndrome Type 3 with Coexistent Universal Dyschromia—An Uncommon Association of a Rare Entity
Griscelli syndrome type 3 is an autosomal recessive disorder caused by mutations in the melanophilin gene and does not have any mucocutaneous or systemic abnormalities other than a pigmentary dilution of skin and hair. We report a case of an 8-year-old girl who presented with silvery grey hair of sc...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer - Medknow
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7678511/ https://www.ncbi.nlm.nih.gov/pubmed/33235850 http://dx.doi.org/10.4103/idoj.IDOJ_572_19 |