Reported about 1 year ago
Angelman Syndrome is caused by genetic mutations or deletions in the 15th pair of chromosomes, typically inherited from the mother. Symptoms include severe developmental delays, unique facial features, and neurobehavioral issues like uncontrollable laughter and involuntary movements. Diagnosis involves genetic testing and counseling to determine the cause. Early signs may not be obvious, but parents should monitor for delayed development, abnormal appearance, and symptoms like seizures. While there is no cure, treatment focuses on symptom management to improve functionality and quality of life.
Source: YAHOO