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Williams Syndrome, also called “Williams-Beuren Syndrome,” is a rare condition caused by missing some genes in our body’s blueprint. It makes some things different for kids who have it, like their appearance, heart health, and how they think. They are often very good at talking and remembering words but might find it harder to understand some things like shapes and numbers.
What is Williams Syndrome?
Williams Syndrome is a rare genetic condition characterized by distinct facial features, developmental delays, cardiovascular issues, and unique social and emotional traits.
What causes Williams Syndrome?
Williams Syndrome is caused by a deletion of genetic material on chromosome 7.
How common is Williams Syndrome?
Williams Syndrome occurs in approximately 1 in 10,000 births worldwide.
What are the physical characteristics of Williams Syndrome?
Individuals with Williams Syndrome often have a broad forehead, puffiness around the eyes, a short nose with a flattened nasal bridge, and a wide mouth with full lips.
Williams Syndrome, scientifically known as Williams-Beuren Syndrome (WS), is a rare genetic disorder caused by the deletion of genetic material on chromosome 7. It is characterized by distinct facial features, cardiovascular abnormalities, and a unique cognitive profile. Individuals with Williams Syndrome often exhibit strengths in verbal skills and face challenges in areas such as visuospatial abilities and mathematical reasoning.
Goally, a tablet-based tool, offers a range of apps designed to assist children with Williams Syndrome in various aspects of their development. These apps can provide support in areas such as building daily routines, fostering language and communication skills, promoting emotional regulation, and developing executive functioning abilities. By incorporating Goally into their daily lives, parents and caregivers can provide their children with engaging and effective tools to enhance their growth and overall well-being.
