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Down syndrome, also known as trisomy 21, is a genetic disorder that occurs when there is an extra copy of chromosome 21. It is one of the most common genetic conditions in children. Down syndrome affects individuals differently but is associated with certain characteristic features and potential health issues. Here are key points to understand about Down syndrome in children:
Genetic Cause:
Diagnosis:
Cognitive and Developmental Impact:
Health Concerns:
Early Intervention:
Educational Considerations:
Inclusion and Support:
Lifespan and Independence:
Genetic Counseling:
It’s important to recognize that each child with Down syndrome is unique, and their abilities and challenges vary. With early intervention, appropriate healthcare, and a supportive environment, children with Down syndrome can achieve their full potential and lead meaningful lives.
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