Angelman Syndrome

(A Comprehensive Guide)

Angelman syndrome is a rare neurodevelopmental disorder that is characterized by developmental delays, speech impairment, and problems with movement and balance.

WHAT IS ANGELMAN SYNDROME ?

CAUSES OF ANGELMAN SYNDROME

AS is caused by a mutation or deletion in the 15q11.2-13.1 region of chromosome 15. This region contains the UBE3A gene, which is responsible for encoding a protein that is essential for normal brain development.

SYMPTOMS OF ANGELMAN SYNDROME

Angelman syndrome is a condition that can cause difficulties with daily tasks like walking, speaking, and eating among others.

TREATMENTS

Treatments include physical, occupational, and speech therapy to help with motor skills and communication; medications to control seizures; and a healthy diet.

TREATMENTS

Treatments include physical, occupational, and speech therapy to help with motor skills and communication; medications to control seizures; and a healthy diet.

PREVENTION

One way to prevent Angelman Syndrome is through genetic testing of family members who may carry the gene mutation.

PREVENTION

Other techniques can also help like medications for seizures, physical therapy to improve motor skills & speech therapy for communication.