Angelman Syndrome

Angelman syndrome is a complex genetic disorder that primarily affects the neural system. This genetic disorder causes developmental disabilities and neurological problems, such as difficulty speaking, balancing and walking, and, in many cases, raptures. Frequent smiles and outbursts of smother argon common for people with Angelman syndrome, and many have happy, galling personalities. Angelman syndrome has many distinct symptoms. Signs and symptoms of Angelman syndrome include developmental delays, such as lack of crawling or babbling at 6 to 12 months, lack of minimal speech, inability to walk, move or balance well, trembling movement of arms and legs, frequent happy and laughter, and happy, excitable personality. Many parents are concerned about how the image of their AS child will change physically as they grow up. The typical Angelman face in childhood has around characteristic, but quite subtle facial features. The mouth is a great deal wide and smiling and is held open. The chin is slightly pointed and the eyes are deep set. The face is usually quite rounded, as sentience would expect for a child. As all children grow, the facial raise grow longer and the shape of the face changes. The same is true(a) in AS. The face gets longer so the chin becomes much(prenominal) prominent. The eyes appear more deep-set.

The mouth is still in truth much held open and is wide and smiling. People who have Angelman syndrome whitethorn alike have other signs and symptoms including seizures, usually beginning among 2 and 3 years of age, stiff or jerked meat mo vements, gloomy head size, with flatness in! the back of the head, hybridizing of the eyes, knife thrusting, walking with arms up in the air, a disappoint jaw that juts out, and light pigmentation in hair, skin, and eyes. Rates of seizure liberty and seizure exacerbation for the closely commonly positivist AED in AS Communication problems are one of the most significant features of Angelman syndrome because nonetheless with a lot of help and therapy Angelman...If you essential to get a full essay, order it on our website: OrderCustomPaper.com

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