Down Syndrome is a genetic disorder that affects people of all ages, but can often be noticed in children shortly after they are born. It is most commonly detected through a physical exam, and the signs and symptoms can vary in severity from person to person.
In general, signs and symptoms of Down Syndrome can be identified in children at the age of two or three months. At this age, a child may display physical features such as a flattened face, a short neck, almond-shaped eyes, a small head, and a protruding tongue. These physical features can be used to diagnose Down Syndrome. Other signs of Down Syndrome may include developmental delays, intellectual disabilities, and delayed motor skills.
In addition, some children with Down Syndrome may have heart defects, hearing loss, vision problems, and thyroid issues. These can be identified through specialized tests that are done when a child is diagnosed with Down Syndrome.
It is important to note that the signs and symptoms of Down Syndrome can vary from person to person, and some individuals may not have any noticeable signs until they are older. If you have any concerns about your child’s development or physical features, it is best to speak with your doctor and get a diagnosis as soon as possible. Early intervention can help children with Down Syndrome to reach their maximum potential.