Williams syndrome is usually caused by a random genetic mutation, or error, in chromosome 7.
Below is a quick explanation of Williams syndrome, what we call our "elevator speech," which is often just enough to share People with Williams syndrome have a 50% chance of passing the condition on to each of their offspring. Williams syndrome is inherited and sometimes spontaneous. Development that is delayed. This means that most people with Williams syndrome have not inherited the condition from a parent.
Our video shown explains Williams syndrome and can be shared to help others understand Williams syndrome.
Williams Syndrome Symptoms. This condition is characterized by mild to moderate intellectual disability or learning problems, unique personality characteristics, distinctive facial features, and … However, sometimes we want to share quick information about WS to people we meet and video might not be feasible. Sings and symptoms of Williams syndrome include *Williams syndrome definition and facts medical author: Charles Patrick Davis, MD, PhD Williams syndrome is a disorder in development that usually results in learning problems, attention deficit disorder, anxiety, and phobias but affected individuals have outgoing personalities.
Feeding problems such as reflux, colic as well as vomiting; Williams syndrome is a developmental disorder that affects many parts of the body.
Signs and symptoms of this disorder include the following: Speech which is delayed but later might turn into strong speaking and learning abilities by hearing. Williams Syndrome is a rare genetic disorder with characteristic features, signs, and symptoms like digestive and eye problems, low birth weight, and cardiac abnormalities. Attention deficit disorder. Symptoms of Williams syndrome can be treated, but there is no cure.
A more detailed explanation follows. Problems with chromosome 7 causes the condition. Williams syndrome is a rare genetic disorder that causes a variety of symptoms and learning issues.