« Albinism »: in fact a symptom part of Albinism and of a number of syndromes
- Albinism is a rare genetic condition affecting around 1 out of 17000 individuals (can vary geographically).
- Albinism is characterized by severe and handicapping deficits in the visual system in association with a most variable hypopigmentation phenotype: visual defects include: foveal hypoplasia, reduced pigmentation of retinal pigment epithelium cells, misrouting of the optic nerves at the chiasm, reduced pigmentation in the iris, photophobia and nystagmus.
- Hypopigmentation may affect the eyes, skin and hair (oculocutaneous albinism, OCA), or be limited to the eyes (ocular albinism, OA).
- Also, there are several syndromic forms of albinism (e.g., Hermansky-Pudlak and Chediak-Higashi syndromes) in which the described hypopigmented and visual phenotypes coexist with more severe pathological alterations.
- To date, mutations in up to 18 genes have been associated with different types of albinism.
- a new locus has been found to be associated with OCA (called OCA5): it has been mapped to the 4q24 human chromosomal region (but the gene itself has not been identified yet).
- OCA6 and OCA7 occur when new genes are mutated SLC24A5 and C10orf11 respectively.
Dr Christophe Hsu – dermatologist. Geneva, Switzerland
Source of information: 2014 (09) – Increasing the Complexity: New Genes and New Types of Albinism. Lluis Montoliu, Mónica Martínez-García, Almudena Fernández. nternational Pigment Cell Conference (IPCC). Singapore