Understanding Down Syndrome
What Is Down Syndrome (Trisomy 21)?
Down syndrome is a genetic condition that occurs when a person is born with an extra copy of chromosome 21—known as Trisomy 21. This additional chromosome alters typical development, leading to a variety of physical, cognitive, and behavioral differences. Individuals with Down syndrome often share recognizable facial features and may experience learning delays or intellectual disabilities that range from mild to moderate. Despite these challenges, many lead fulfilling lives, especially when supported by early intervention and appropriate therapies.
Developmental, Neurological, and Physical Challenges
People with Down syndrome commonly face a wide range of developmental and health-related challenges, including:
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Delayed motor skills and speech development
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Learning difficulties and slower cognitive processing
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Heart defects present at birth
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Vision and hearing impairments
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Increased likelihood of developing Alzheimer’s disease later in life
Many of these complications are linked to how the extra chromosome affects brain development, immune function, and other systems throughout the body.
Why Traditional Therapies Often Fall Short
Conventional treatments—such as physical therapy, occupational therapy, speech-language intervention, and specialized education—can help children with Down syndrome develop essential skills. However, these approaches primarily focus on symptom management rather than addressing the underlying biological issues caused by the extra chromosome. As a result, progress can be slow and limited. This gap in care has driven growing interest in regenerative medicine—especially exosome therapy, which holds promise for targeting cellular and neurological dysfunction at its core.