SciELO - Scientific Electronic Library Online

 
vol.11Profile and opinion of people with disability with respect to adapted physical activity participation in Ethiopia índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Articulo

Indicadores

Links relacionados

  • En proceso de indezaciónCitado por Google
  • En proceso de indezaciónSimilares en Google

Compartir


African Journal of Disability (Online)

versión On-line ISSN 2226-7220
versión impresa ISSN 2223-9170

Resumen

KROMBERG, Jennifer G.R.  y  KERR, Robyn. Oculocutaneous albinism in southern Africa: Historical background, genetic, clinical and psychosocial issues. Afr. j. disabil. (Online) [online]. 2022, vol.11, pp.1-7. ISSN 2226-7220.  http://dx.doi.org/10.4102/ajod.v11i0.877.

Albinism is an inherited condition associated with significant depigmentation of the skin, hair and eyes. It occurs in every population with varying frequency, and narratives of people with albinism have been recorded since 200 BC. In southern Africa albinism is common, about 1 in 4000 people are affected, but it remains a poorly understood condition surrounded by myths and superstition. This article provides a historical background on oculocutaneous albinism (OCA) in southern Africa and presents relevant information from the literature regarding epidemiology, genetics and genetic counselling, health, psychosocial and cultural issues, and medical care. There are several recessively inherited types of OCA and a mutation, responsible for about 80% of South African variants, has been identified in OCA type 2. The physical characteristics associated with albinism, that is, sun-sensitive skin and low vision, can be managed. However, people with OCA in Africa also experience psychosocial issues, such as discrimination, because of the various superstitious beliefs and attitudes held in the community. Management should include medical care for health problems, appropriate adjustment of the schooling context and genetic counseling. In addition, widespread public awareness programmes are required to increase the knowledge of the genetic causes of OCA and of the nature of genetic counselling, to address the negative attitudes in the community, to reduce the marginalisation and stigmatization of people with albinism and to improve their quality of life.

Palabras clave : albinism and Africa; clinical management; culture; disability; epidemiology; genetics; genetic counselling; health; oculocutaneous albinism; psychosocial issues.

        · texto en Inglés     · Inglés ( pdf )

 

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons