The parents of an adorable toddler who suffers from a rare syndrome with no known cure that leaves him crippled each time he gets a cold or flu are fighting to find a cure for their son in an online campaign.
Two-year-old Roberto from the city of Algeciras in the province of Cadiz, Spain, is one of the thirty people around the globe currently reported to be suffering from Capos Syndrome, a neurological disorder caused by the mutation of a gene known as ATP1A3.
The disease symptoms trigger each time he gets a disease causing fever, making it difficult for him to control his body, causing hearing and sight difficulties and cognitive problems. Typically it improves when the disease that triggered the symptoms ends.
There is no known cure for the syndrome that does not have any definite prognosis but can affect the heart and result in brain damage, blindness and hearing loss.
In an interview with Zenger News, Roberto’s mother, Demelsa Gonzalez Perez, 42, explained that Capos Syndrome episodes begin with a fever along with ataxia, a series of disorders that affect coordination, balance and speech.
She added: “After a feverish episode, my son began to convulse and at first they thought it was an autoimmune encephalitis, after ruling it out with tests, they carried out genetic tests in Barcelona and got the final diagnosis.”
According to Gonzalez Perez, the University of Southwestern in Texas studied the modification of the affected gene but no news has come of this research since 2019.
Roberto’s father, Ruben, told local media that the toddler’s nineteen-year-old sister is also having a hard time with the situation.
He added: “We’ve really only known what’s been going on since May and it’s hard to process.”
Gonzalez Perez, a grocery market employee and concerned mother of two decided to launch an online campaign in the hopes that it will bring her family closer to finding a cure for Roberto.
Gonzalez Perez writes: “I am launching this campaign because I need help, it is important to find information that will allow me to better understand my son’s condition.
“It is also urgent that I find alternatives to treat him and improve his quality of life.
“At this time any contribution would be very valuable for my family, if anyone knows about the syndrome or has the contact details of other patients or foundations that can help me with guidance on the disease, I would greatly appreciate it.
“I need support in order to get a response, so if you can help me by signing and sharing, that would be great.”
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