Prevalence of congenital colour vision deficiency among Black school children in Durban, South Africa

OBJECTIVES: Congenital colour vision deficiency (CCVD) is an x-linked chromosome disorder that results from abnormalities in one or all three-cone type’s photoreceptors. Early assessment and diagnosis of CCVD is necessary to minimise the disability associated with the condition. Multistage sampling...

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Detalles Bibliográficos
Autores principales: Mashige, Khathutshelo Percy, van Staden, Diane Beverly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558866/
https://www.ncbi.nlm.nih.gov/pubmed/31182158
http://dx.doi.org/10.1186/s13104-019-4374-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558866/
https://www.ncbi.nlm.nih.gov/pubmed/31182158
http://dx.doi.org/10.1186/s13104-019-4374-1

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