Angelman Syndrome

Angelman syndrome is a complex genetic disorder that primarily affects the sickish system. This genetic disorder causes developmental disabilities and neurological problems, such as difficulty speaking, balancing and walking, and, in many cases, captures. Frequent smiles and outbursts of joke are common for people with Angelman syndrome, and many have happy, sensitive 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 delighted and laughter, and happy, excitable personality. Many parents are concerned about how the denominate of their AS child will change physically as they grow up. The typical Angelman face in childhood has many characteristic, but quite subtle facial features. The mouth is frequently 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 admirer would expect for a child. As all children grow, the facial pearl grow longer and the shape of the face changes. The same is transparent in AS. The face gets longer so the chin becomes often prominent. The eyes appear more deep-set. The mouth is still actually much held open and is wide and smiling. People who have Angelman syndrome may alike have other signs and symptoms including seizures, usually beginning among 2 and 3 years of age, stiff or jerk movements, gloomy head size, with flatness in the back of the head, crisscross 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 well-nigh commonly plus AED in AS Communication problems are one of the most significant features of Angelman syndrome because nonetheless wi! th a lot of help and therapy Angelman...If you want to get a full essay, order it on our website: OrderCustomPaper.com

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