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Angelman syndrome is a genetic disorder that mainly affects the nervous system. Angelman syndrome is due to a lack of function of part of chromosome 15 inherited from a persons mother. it is due to a deletion or mutation of the UBE3A gene on that chromosome.
Symptoms include a small head and a specific facial appearance, severe intellectual disability, developmental disability, speaking problems, balance and movement problems, seizures, and sleep problems these symptoms can be noticed after a one year after birth and is diagnosed based on symptoms and possibly genetic testing and has no cure is
Medications include Anti-seizure medications are used in those with seizures, Physical therapy and bracing may help with walking
Neurophysiology and Rehabilitation emphasize in publishing the original scholarly articles related to Neurology and Rehabilitation worldwide. The journal follows rapid review process with the Eminent Editorial Board
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