Albinism – symptomatology, aetiology, and therapy
Albinism is a rare, genetically determined disorder of melanogenesis resulting in a reduction or complete absence of melanin in tissues of ectodermal origin, especially skin, hair, and irises of the eyes. It may occur in isolated form as oculocutaneous albinism inherited in an autosomal recessive ma...
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| Egile Nagusiak: | , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
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Termedia Publishing House
2025-03-01
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| Saila: | Pediatria Polska |
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| Sarrera elektronikoa: | https://www.termedia.pl/Albinism-symptomatology-aetiology-and-therapy,127,55703,1,1.html |
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