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Down Syndrome
A genetic condition caused by an extra copy of chromosome 21 that can affect development, learning, and health in different ways.
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Turner Syndrome​
A genetic condition involving a missing or altered X chromosome that can affect growth, development, and other areas of health.
​Fragile X Syndrome
A genetic condition that can affect learning, development, communication, and behavior.
Williams Syndrome
A genetic condition caused by a change in chromosome 7 that can affect development, learning, the heart, and other areas of health.
​Prader-Willi Syndrome
A genetic condition that can affect growth, development, muscle tone, metabolism, and regulation of hunger.
​Angelman Syndrome
A genetic condition affecting the nervous system that can impact development, speech, movement, and balance.
22q11.2 Deletion Syndrome
A genetic condition caused by a deletion on chromosome 22 that can affect multiple body systems, including the heart, immune system, development, and learning.
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