[The affected area of chromosome is known as the Williams-Beuren syndrome critical region (WBSCR) and encompasses the elastin gene (ELN). Genetic testing is often used to confirm a diagnosis of Williams syndrome. I am looking to understand more about Williams syndrome. In most cases, the gene changes (mutations) occur on their own, either in the sperm or egg that a baby develops from. Someone can help me? One of the characteristics of Williams syndrome is an inappropriate increase in social behavior. Williams syndrome is a neurodevelopmental disorder characterized by hypersociability and unique neurocognitive abnormalities. Management may include: Feeding therapy for infants with feeding problems; Early intervention programs and special education programs for children with varying degrees of developmental disabilities; Behavioral counseling and/or medications … LOOKING TO UNDERSTAND MORE ABOUT WILLIAMS SYNDROME AND POSSIBLE TREATMENT OPTIONS. Treatment for the condition tends to involve addressing the symptoms that the condition causes to help improve and maintain the patient’s quality of life. The treatment only focuses on easing the symptoms associated with the problem. Williams Syndrome describes the condition of a person who has an entire chromosome arm missing from their DNA. Virtual Convention 10/12/2020 . Regular checkups help your healthcare provider in keeping track of arising problems. These treatments basically ease the symptoms of Williams syndrome to bring considerable relief. Intake of excessive … Special Ed, as well as occupational therapy, improves these individuals school … Williams syndrome cannot be cured. However it is said that person which this medical condition needs regular cardiovascular monitoring for other potential problems such as narrowing of the blood vessels, … There are several ways for individuals to handle their incapacities. This condition is … Treatment Options For Williams Syndrome. Treatment. Treatment of Williams syndrome. Specifically, the Williams syndrome, clinically, is characterized by 4 cardinal points: 1) atypical features and facial features , 2) generalized retardation of psychomotor development … Suite 223 Troy, MI 48084-4153. info@williams-syndrome.org. It is likely that the elastin gene In most families, the child with Williams syndrome is the only one to have the condition in his or her entire extended family. Williams Syndrome Treatment There is no known cure for the Williams Syndrome nor a particular treatment inasmuch the treatment usually depends on the symptoms manifesting from one person to another. Prader-Willi syndrome is a rare genetic disorder that results in physical, mental and behavioral problems, including a constant sense of hunger. One of the 25 missing genes is the gene that produces elastin, a protein that allows blood vessels and other tissues in the body to stretch. One of the missing genes is the gene that … Treatments are based on an individual’s particular symptoms. You need to understand that the condition has no cure. This includes speech therapy and physical therapy that can help make the patient as functional as possible. Children with Williams syndrome who have a heart defect may need heart catheterization or surgery to repair the … The Williams Syndrome (WS) is a developmental disorder of genetic origin that is associated with a characteristic profile of physical and cognitive affectations (Galaburda et al., 2003). Repairing surgeries are done for correcting heart valve leakage and septal defects. Williams syndrome … This session will discuss the signs and treatments for each. Treatment. Genetic causes, treatments, and life expectancy information are provided.