In South Africa, 19-year-old Beandri Bea, who lived with Hutchinson-Gilford syndrome, died of complications – a rare genetic disease that causes extremely rapid aging of the body.
This is reported by Daily Mail. Beandri was the last known patient in South Africa with this pathology.
What is Hutchinson-Gilford Syndrome?
It is a rare genetic mutation that affects about one in four million newborns. The disease, also known as progeria, causes the body to age rapidly, accompanied by numerous health problems, including osteoporosis, which makes bones extremely fragile.
Despite the difficulties caused by the disease, Beandri Bea inspired many with her optimism and zest for life.
“My goal is to raise awareness of people with special needs and show that each of us is unique”, — she shared with her followers on social media.
Two months ago, the girl underwent open-heart surgery and was in the process of rehabilitation. She had hoped to spend Christmas with her parents, but due to the severity of the illness, this became impossible.
Beandri's mother confirmed her death and thanked everyone who supported her daughter.
“Despite all the difficulties, Beandri always radiated joy and hope. She inspired those who knew her with her strong spirit”, — she said.
Unfortunately, most people with progeria rarely live past 20 years of age, as the disease significantly limits life expectancy.
Beandri's death is a reminder of the importance of research and raising awareness about rare diseases that affect the quality and length of life.