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Williams syndrome

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Williams-Beuren syndrome; WBS; Beuren syndrome; 7q11.23 deletion syndrome; Elfin facies syndrome

Definition

Williams syndrome is a rare disorder that can lead to problems with development.

Causes

Williams syndrome is caused by not having a copy of 25 to 27 genes on chromosome number 7.

In most cases, the gene changes occur on their own, either in the sperm or egg that a baby develops from.
However, once someone carries the genetic change, their children have a 50% chance of inheriting it.

One of the missing genes is the gene that produces elastin. This is a protein that allows blood vessels and other tissues in the body to stretch. It is likely that missing a copy of this gene results in the narrowing of blood vessels, stretchy skin, and flexible joints seen in this condition.

Symptoms

Symptoms of Williams syndrome are:

Feeding problems, including colic, reflux, and vomiting
Inward bend of the small finger
Sunken chest
Heart disease or blood vessel problems
Developmental delay, mild to moderate intellectual disability, learning disorders
Delayed speech that may later turn into strong speaking ability and strong learning by hearing
Easily distracted, attention deficit hyperactivity disorder (ADHD)
Personality traits including being very friendly, trusting strangers, fearing loud sounds or physical contact, and being interested in music
Short height, compared to the rest of the person's biologic relatives

The face and mouth of someone with Williams syndrome may show:

A flattened nasal bridge with small, upturned nose
Long ridges in the skin that run from the nose to the upper lip
Prominent lips with an open mouth
Skin that covers the inner corner of the eye
Partially missing teeth, defective tooth enamel, or small, widely spaced teeth

Exams and Tests

Tests for Williams syndrome include:

Blood pressure check
Genetic testing, such as a blood test for a missing piece of chromosome 7 (FISH test or microarray)
Urine and blood tests for calcium level
Echocardiography combined with Doppler ultrasound
Kidney ultrasound

Exams and tests may find the following signs:

Narrowing of some blood vessels
Farsightedness
Dental problems, such as teeth that are widely spaced
High blood calcium level that may cause seizures and rigid muscles
High blood pressure
Loose joints that may change to stiffness as the person gets older
Unusual star-like pattern in iris of the eye

Treatment

There is no cure for Williams syndrome. Avoid taking extra calcium and vitamin D. Treat high blood calcium if it occurs. Blood vessel narrowing can be a major health problem. Treatment is based on how severe it is.

Physical therapy is helpful for people with joint stiffness. Developmental and speech therapy can also help. For example, having strong verbal skills can help make up for other problems. Other treatments are based on the person's symptoms.

It can help to have treatment coordinated by a geneticist who is experienced with Williams syndrome.

Support Groups

More information and support for people with Williams syndrome and their families can be found at:

Williams Syndrome Association -- williams-syndrome.org

Outlook (Prognosis)

Most people with Williams syndrome:

Have some intellectual disability.
May have a shortened lifespan due to the various medical issues and other possible complications.
Require full-time caregivers and often live with supervision.

Possible Complications

Complications may include:

Calcium deposits in the kidney and other kidney problems
Death (in rare cases from anesthesia)
Heart failure due to narrowed blood vessels
Pain in the abdomen

When to Contact a Medical Professional

Many of the symptoms and signs of Williams syndrome may not be obvious at birth. Contact your health care provider if your child has features similar to those of Williams syndrome. Seek genetic counseling if you have a family history of Williams syndrome.

Prevention

There is no known way to prevent the genetic problem that causes Williams syndrome. Prenatal testing is available for couples with a family history of Williams syndrome who wish to conceive.

References

Bockenhauer D. Fluid, electrolyte, and acid-base disorders in children. In: Yu ASL, Chertow GM, Luyckx VA, Marsden PA, Skorecki K, Taal MW, eds. Brenner and Rector's The Kidney. 11th ed. Philadelphia, PA: Elsevier; 2020:chap 73.

Morris CA. Williams syndrome. In: Adam MP, Feldman J, Mirzaa GM, et al, eds. GeneReviews. University of Washington, Seattle, WA. www.ncbi.nlm.nih.gov/books/NBK1249/. Updated April 13, 2023. Accessed April 19, 2024.

National Organization for Rare Disorders website. Williams syndrome. rarediseases.org/rare-diseases/williams-syndrome/. Accessed April 19, 2024.

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Review Date: 12/31/2023

Reviewed By: Anna C. Edens Hurst, MD, MS, Associate Professor in Medical Genetics, The University of Alabama at Birmingham, Birmingham, AL. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.

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