Family races to help 2 sons who could die of rare disease by age 10
When Jennie and Gary Landsman learned their sons had a fatal, rare disease, they started fundraising to support a gene therapy to help their sons and others.When Jennie Landsman's son Benny was 6 months old, she noticed he struggled to sit up, roll over or scoot like other babies. Worried, she took him to a neurologist.
Mom leads fight for son with rare disease . Sandra Sermone is a mother on a mission . She is determined to know everything about her 10-year-old There is currently no cure for ADNP syndrome, but the FDA has given special designation to a new drug which could be the first possible treatment
Sandra Sermone says her son is one of 11 children in history to be diagnosed with ADNP syndrome, an autism-related disorder . When Sandra Sermone gave birth to her son Tony 10 years ago, she was devastated to learn that he had several heart defects. Little did she know, the abnormalities would be
Sandra Sermone is a mother on a mission. She is determined to know everything about her 10-year-old son's .
"He has brain abnormalities, heart abnormalities. He had feeding problems, gross motor, fine motor, and oral motor delays," Sermone told CBS News.
Her son, Tony, was born with ADNP syndrome, an autism-related genetic disorder so rare that four years ago, only 10 other cases in the world had been diagnosed. When she looked for more information, she learned there was only one study about the disorder.
"I read that publication probably 50 times," Sermone said. "And I ended up saying I need to find these 10 parents."
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One family’ s desperate race to find a cure for a condition that mimics Parkinson’ s and Alzheimer’ s — and plagues their 2 ¹/₂-year-old son . Only about 150 children worldwide are currently diagnosed with the disease . Like other neurodegenerative diseases , it leads to a dangerous iron buildup in patients’
Cure Rare Disease has teamed up with local fire departments for our Bucks in the Bucket campaign. Firefighters volunteer their time to collect money on the Our collaborations strive to accelerate cures for rare genetic disorders including but not limited to Muscular dystrophies (Duchenne, Limb-girdle
She created her own database, website and patient registry, which has now identified more than 150 other children with the same condition.
Recently, some of those families met face to face.
"It's very emotional. A lot of times you feel like you are alone as parents," Victoria Malvagno said.
Another parent, Genie Egerton-Warburton, said being in the same room "with all these children and all these parents who are living what we have been through is heartwarming and amazing."
February 28 marks . A disease like ADNP syndrome is considered rare if it affects fewer than 200,000 people.
After connecting with Sermone, researchers at Mount Sinai Hospital in New York City are launching a new study on the condition that affects her son.
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Her son Tony was born with ADNP syndrome, an autism-related genetic disorder . It’ s so rare that four years ago, only 10 other There is currently no cure for ADNP syndrome, but the FDA has given special designation to a new drug that could be the first treatment for patients with the rare disease .
Olivia Burtwistle grew as a typically curious and energetic child until soon after her fourth birthday, when her parents began to notice changes, including a “rapid decline” in Olivia’ s vision. At age 7, their daughter was diagnosed with juvenile Batten disease , a rare genetic illness that affects children.
"[We're] trying to figure out the biology of this disorder and other similar disorders, so that we can come up with new drugs that are targeted to the disorder," said Dr. Joseph Buxbaum, director of the Seaver Autism Center at Mount Sinai.
Sermone has even authored five research papers with her own findings.
"Even if it's not for Tony, if one family -- if one day they can make this stop or find out what's causing it, it will all be worth it," she said.
There is currently no cure for ADNP syndrome, but the FDA has given special designation to a new drug which could be the first possible treatment for patients with the rare disease.
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What Is Ocular Melanoma? .
<p>Doctors are puzzled after two groups of people in Huntersville, North Carolina and Auburn, Alabama were diagnosed with a rare form of eye cancer. The strange part? Some of them were friends who attended the same college, CBS News reports.</p>Juleigh Green began seeing strange flashes of light when she was 27 years old. Her friend Allison Allred started experiencing similar symptoms at 31. Both women were diagnosed with ocular melanoma and needed to have an eye removed. After their friend Ashley McCray noticed black spots in her iris, she too received the same diagnosis. All three of them attended Auburn University together.