Angelman syndrome is a genetic disorder that mostly affects boys and typically shows symptoms in infancy or early childhood. Some of the more common symptoms include clumsiness, jerky movements, speech problems, hyperactivity and extreme shyness.
Introduction
Angelman syndrome is a genetic disorder that affects the development of the central nervous system. The effects of this disease include developmental delays and movement disorders. Symptoms include jerky movements, difficulty with walking, and tremors. There are two types of Angelman syndrome: 1) Early-onset, which is characterized by poor muscle tone; 2) Late-onset, which is characterized by intellectual disability.
What is Angelman Syndrome?
Angelman Syndrome is a genetic disorder that causes developmental disabilities and learning disabilities. It is caused by an unstable copy of the chromosome 15. Symptoms will vary from person to person, but they may include the following:
– difficulties with motor coordination
– repetitive hand movements
– hyperactivity
– epilepsy
– developmental delay
– sleep problems
– emotional problems.
It occurs in one of every six thousand people. Angelman Syndrome affects boys and girls equally.
Who is at risk for Angelman Syndrome? Angelman syndrome is a genetic disorder that affects males and females equally. Usually it occurs in the first or second trimester of pregnancy, but it can also occur after birth, so parents should be aware that there may be symptoms of autism during infancy. R
Where does the syndrome occur?
Angelman syndrome is a genetic disorder that affects many parts of the body. It is most common in boys and usually occurs before or during birth. Symptoms include severe delays, lack of social skills, and if left untreated, can lead to death. What causes Angelman syndrome?. Angelman syndrome is caused by a genetic mutation in a single gene. The mutation affects the function of a protein called UBE3A, which plays an important role in the brain and nervous system. In some cases, changes in other genes are also present that may cause other symptoms.
What are the characteristics of the syndrome?
Angelman Syndrome is a genetic disorder that affects the development of the brain. It is more prevalent in males than females and can cause jerky movements, high-pitched screams, and seizures. Angelman Syndrome is also known as the happy face syndrome because of the way people with this condition often display a wide smile on their faces.
Symptoms of Angelman Syndrome
Angelman Syndrome is a genetic disorder that controls brain function. Symptoms include delayed language and speech development, hypotonia (inability to move), and social impairment that makes it difficult for children with Angelman Syndrome to communicate or interact with their friends. The most common symptom of this disorder is an outward lack of emotion, which can be seen as happy and giddy instead of sad or angry.
Treatment for Angelman Syndrome
Angelman syndrome is a rare genetic disorder that occurs in the brain. It is caused by a mutation on the 15th chromosome. There are two types of Angelman syndrome, and both are associated with seizures. Children who have Angelman syndrome often have developmental delays, intellectual impairment, and motor skill difficulties. The main treatment is speech and language therapy given by a therapist. A child with Angelman syndrome may respond to certain drugs, but this is not yet known. Other treatments include: physical therapy, occupational therapy, and sensory stimulation.
Children with Angelman syndrome can have seizures and may need to take seizure medication during the day or at night. Siblings of children with Angelman syndrome are more likely to develop the disorder if they are born to a mother who has an Angelman syndrome-like condition. Ten percent of children with Angelman syndrome have another type of genetic disorder called Mowat-Wilson Syndrome in which the child also has intellectual disability and seizures.
Durga Awasthi 
Sonal Mitra 
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