Family 'over the moon' with Southampton albinism research funding
"It's really exciting to imagine how many children could benefit in the years to come."
Albinism affects between one in 12,000 and one in 15,000 people in European countries, and affects the production of melanin - pigment which colours eyes, skin and hair.The condition is associated with a deficiency of a chemical called L-DOPA, which is essential for the normal development of retinas.As a result, babies with albinism can have severe sight problems as they grow up.For years, Dr Helena Lee has looked at whether replacing L-DOPA could improve eye development.Her research project, called OLIVIA, has been granted £542,000 from the Medical Research Council to investigate whether Levodopa could hold the key if given to children below the age of two."We believe we've found a treatment which will help [children with albinism], and this award means we can start testing this in the real world," said Dr Lee.
Abbey and another parent, Joe, whose daughter also has albinism, have already raised over £43,000 to help support the study.Joe, whose two-year-old daughter Raya wears glasses for short-sightedness to protect her eyes, completed seven marathons in seven cities in seven days in aid of the University charity, Gift of Sight."News of this new funding to allow trials to go ahead is fantastic," he said.The university said the OLIVIA study, which is set to begin as a small-scale trial with about 10 children, could also pave the way for identifying new therapies for other childhood eye conditions.
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