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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...
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| Publicado no: | Indian Dermatol Online J |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer - Medknow
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7678511/ https://ncbi.nlm.nih.gov/pubmed/33235850 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/idoj.IDOJ_572_19 |
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