Gene Therapy-Rare Disease
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Gene Therapy-Rare Disease
Camden Alderman, 21, who has a rare disease called Wiskott-Aldrich syndrome, holds with an infusion pump he uses near his home in Greensboro, N.C., Wednesday, June 12, 2024. When he was a toddler, doctors removed his spleen because of uncontrolled bleeding. As a young boy, he wound up in the hospital many times and was told he couldn’t play baseball. (AP Photo/Chuck Burton)
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Gene Therapy-Rare Disease
Camden Alderman, 21, who has a rare disease called Wiskott-Aldrich syndrome, holds some of the drugs and medical equipment he uses near his home in Greensboro, N.C., Wednesday, June 12, 2024. (AP Photo/Chuck Burton)
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Gene Therapy-Rare Disease
FILE - This undated image made available by the National Human Genome Research Institute shows the output from a DNA sequencer. Collectively, about 350 million people worldwide suffer from rare diseases, most of which are genetic. But each of the 7,000 individual disorders affects perhaps a few in a million people or less. So there’s little commercial incentive to develop or bring to market these one-time therapies to fix faulty genes or replace them with healthy ones. (NHGRI via AP, File)
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Gene Therapy-Rare Disease
Robin Alderman, right, and her son, Camden Alderman, 21, who has a rare disease called Wiskott-Aldrich syndrome, pose for a portrait near their home in Greensboro, N.C., Wednesday, June 12, 2024. (AP Photo/Chuck Burton)
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Gene Therapy-Rare Disease
Robin Alderman, right, and her son, Camden Alderman, 21, pose for a portrait near their home in Greensboro, N.C., Wednesday, June 12, 2024. Camden, 21, was diagnosed as a baby with a rare disease called Wiskott-Aldrich syndrome, which is caused by a mutated gene on the X chromosome. It primarily affects boys – up to 10 out of every million — and can cause frequent infections, eczema and excessive bleeding. (AP Photo/Chuck Burton)
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Gene Therapy-Rare Disease
Robin Alderman, right, looks up to her son, Camden Alderman, 21, who has a rare disease called Wiskott-Aldrich syndrome, as they pose for a portrait near their home in Greensboro, N.C., Wednesday, June 12, 2024. (AP Photo/Chuck Burton)
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Camden Alderman, 21, who has a rare disease called Wiskott-Aldrich syndrome, holds with an infusion pump he uses near his home in Greensboro, N.C., Wednesday, June 12, 2024. When he was a toddler, doctors removed his spleen because of uncontrolled bleeding. As a young boy, he wound up in the hospital many times and was told he couldn’t play baseball. (AP Photo/Chuck Burton)