Rare tropical skin disease
THE ASSOCIATED PRESS
ARARAS, Brazil — This is a village where the people melt away.
Tucked into the sunbaked rolling hills of Brazil’s midwest, Araras is home to what is thought to be the largest single group of people suffering from a rare inherited skin disease known as xeroderma pigmentosum — or “XP.”
Those with the disease are extremely sensitive to ultraviolet rays from sunlight and highly susceptible to skin cancers — it robs victims of the ability to repair the damage caused by the sun.
That’s a particularly vexing burden in Araras, a tropical farming community where outdoor work is vital for survival.
“I was always exposed to the sun — working, planting and harvesting rice and caring for the cows, ” said Djalma Antonio Jardim, 38. “As the years passed my condition got worse.”
Agriculture is no longer a real option for Jardim. He survives on a small government pension and meagre earnings from an ice cream parlour he runs.
Jardim says he was just 9 when a large number of freckles and small lumps started appearing on his face — the tell-tale signs that experts say signal XP is present in children and call for serious precautions to be taken to protect them against the sun.
Such precaution wasn’t taken for Jardim, who now wears a large straw hat in an effort to protect his face. But it’s helped little. He has undergone more than 50 surgeries to remove skin tumors.
In an effort to camouflage how the disease has eaten away the skin on his lips, nose, cheeks and eyes, Jardim wears a rudimentary orange-tinted mask, its stenciled-in right eyebrow not matching his bushy real one that remains.
Beyond skin damage and cancers that XP patients get, about one in five may also suffer from deafness, spastic muscles, poor co-ordination or developmental delays, according to the U.S.-based National Cancer Institute.
More than 20 people in this community of about 800 have XP. That’s an incidence rate of about one in 40 people — far higher than the one in 1 million people in the United States who have it.
For years, nobody could tell Jardim or the others what was afflicting them.
“The doctors I went to said I had a blood disorder. Others said I had a skin problem. But none said I had a genetic disease, ” Jardim said. “It was only in 2010 that my disease was properly diagnosed.”
Experts say Araras has such a high incidence rate because the village was founded by only a few families and several were carriers of the disease, meaning it was passed to future generations as villagers intermarried.
For instance, both of Jardim’s parents were carriers of the defective gene that causes the disease, largely ensuring he would have it.
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