# data[].attributes.body
Department of Health & Human Services. “Williams Syndrome.” Better Health Channel, Department of Health & Human Services, 30 Aug. 2013, www.betterhealth.vic.gov.au/health/conditionsandtreatments/williams-syndrome.

Herndon, Jaime. “Williams Syndrome: Symptoms, Diagnosis, and Treatments.” Healthline, Healthline Media, 9 July 2017, www.healthline.com/health/williams-syndrome.

“Williams Syndrome Information Page.” National Institute of Neurological Disorders and Stroke, U.S. Department of Health and Human Services, www.ninds.nih.gov/Disorders/All-Disorders/Williams-Syndrome-Information-Page.

“Williams Syndrome.” Genetic and Rare Diseases Information Center, U.S. Department of Health and Human Services, rarediseases.info.nih.gov/diseases/7891/williams-syndrome/cases/22698.

“Williams Syndrome.” NORD (National Organization for Rare Disorders), rarediseases.org/rare-diseases/williams-syndrome/.

“Williams Syndrome: Causes, Symptoms, Diagnosis & Treatment.” Cleveland Clinic, my.clevelandclinic.org/health/diseases/15174-williams-syndrome.

# data[].attributes.body
Individuals with Williams Syndrome may have a shortened life expectancy, but no specific studies exist to determine the exact life expectancy for those with Williams Syndrome. However, there has been humans with the syndrome to live into their 60s. individuals with Williams Syndrome have a 50% chance of having a child with the syndrome due to the inheritance pattern. But most Williams Syndrome occurrences are not inherited and happens due to random events in the pregnancy.

# data[].attributes.body
While there is no cure for Williams Syndrome currently, there is treatments to ease the symptoms of the syndrome. These treatments may include speech therapy, medical monitoring for the heart and blood vessels, social training. These are not always needed in all cases of Williams Syndrome.

# data[].attributes.body
Williams Syndrome is caused by a missing segment of genetic material in chromosome 7.  This means there is no way no prevent your new born to have Williams syndrome.

# data[].attributes.body
- wide mouth
- ADHD
- learning disorders
- speech delays
- widely spaced teeth
- specific phobias
-  puffy eyes
- kidney abnormalalitys
- more oxytocin

# data[].attributes.body
Williams Syndrome is a rare genetic disorder. Which can be identified by growth delays. it effects both males and females. It occurs around once per 10,000 - 20,000 births. individuals with Williams Syndrome are usually diagnosed before the age of 4. The disorder was discovered in 1961 by J.C.P Williams.