Does Williams syndrome get worse with age?

Does Williams syndrome get worse with age?

Williams syndrome, also known as Williams-Beuren syndrome, is a rare genetic disorder characterized by growth delays before and after birth (prenatal and postnatal growth retardation), short stature, a varying degree of mental deficiency, and distinctive facial features that typically become more pronounced with age.

What is the average life expectancy of a person with Williams syndrome?

What Is the Life-Expectancy of Williams Syndrome? Is There a Cure? The average loss of lifespan or life expectancy is estimated to be about 10-20 years, but there is a lack of data to confirm this.

Are people with Williams syndrome slow?

Learning problems are common in children with Williams syndrome. They range from mild to severe. Children are slower to walk, talk, and gain new skills compared to other children their age.

Is Williams Syndrome progressive?

Williams syndrome is a progressive disorder with multisystem involvement.

Does Williams syndrome qualify for disability?

Williams Syndrome is considered to be a disability, however you cannot immediately claim SSI if your child has it because it’s not a listing claim.

What kind of medical assistance is needed for Williams syndrome?

Many individuals with Williams syndrome require early intervention programs, therapies, or special education due to developmental delays and/or learning problems. Individuals with elevated blood calcium levels may need to be seen by a nutritionist or followed by a nephrologist.

What do you need to know about Williams syndrome?

View Full Treatment Information. Definition. Williams Syndrome (WS) is a rare genetic disorder characterized by mild to moderate delays in cognitive development or learning difficulties, a distinctive facial appearance, and a unique personality that combines over-friendliness and high levels of empathy with anxiety.

What are the medical problems associated with WS?

The most significant medical problem associated with WS is cardiovascular disease caused by narrowed arteries. WS is also associated with elevated blood calcium levels in infancy. A random genetic mutation (deletion of a small piece of chromosome 7), rather than inheritance, most often causes the disorder.

When to see a nephrologist for Williams syndrome?

• Renal tract screening to include kidneys and bladder If nephrocalcinosis refer to nephrologist for 6 monthly screening. If structural abnormalities, management or referral as necessary.