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Angelman is a genetic disease so it is not found in certain places. But there are age groups that are affected

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Most cases of Angelman syndrome are not inherited, particularly those caused by a deletion in the maternal chromosome 15 or by paternal uni-parental disomy. These genetic changes occur as random events during the formation of reproductive cells (eggs and sperm) or in early embryonic development. Affected people typically have no history of the disorder in their family.

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You can try to control the disease by using the common treatments like therapy, test, exams, and taking the right medicine.

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Because most cases of Angelman Syndrome are caused by spontaneous genetic mutations, there is currently no known way to prevent the disease.

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Angelman syndrome is caused by mutations or defects in the UBE3A gene on chromosome 15. The UBE3A gene provides instructions for making the enzyme ubiquitin protein ligase E3A. This enzyme is involved in targeting proteins to be degraded, or broken down, within cells.

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side effects include lack of crawling or babbling, minimal speech, and frequent smiling and laughter. Inability to walk, move, or balance well.

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Developmental: delays or abnormal patterns of development in the areas of communication/language, motor skills, problem-solving or social and adaptive behavior.
Learning: Difficulty with specific subjects, organizing, behavioral problems, comprehending, and often result in academic underachievement.
Medical: medical problems/ concerns
Mental health: problems with adjustment, anxiety, depression, coping, behavior etc.

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Treatment includes anti-seizure medication and therapies to help manage medical and developmental concerns.Treatment can help, but this condition can't be cured. It requires a medical diagnosis, Lab tests or imaging often required.
listed below are a few treatments:
Anticonvulsant drugs
Assisted-mobility devices
Behavioral therapy
Dental care
Education
Ketogenic diet
Occupational therapy
Stimulant drugs
Sedative drug

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Angelman syndrome is a complex genetic disorder that primarily affects the nervous system.