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Treatment and Prevention Allan-herndon-dudley Syndrome

Have you ever wondered if what you know about Allanherndondudley, Complete, Information, Prevention, Syndrome, Treatment is accurate? Consider the following paragraphs and compare what you know to the latest info on Allanherndondudley, Complete, Information, Prevention, Syndrome, Treatment.

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Allan Herndon Dudley syndrome is a rare disease of the mind that the growth of conservative severe mental retardation and problems with the causes of the campaign. This fact, which occurs exclusively on men involved, growth in the period before birth. Allan Herndon Dudley syndrome, severe mental retardation, a reduced ability to organize and speak naturally words (dysarthria characterized), reduced muscle color, and abnormalities of the campaign. This fact, which occurs exclusively on men involved, growth in the period before birth. Consequently, many people with Allan Herndon Dudley syndrome are unable to walk independently and engaged in a wheelchair after the due date. Most children with Allan Herndon Dudley syndrome have low muscle color and underdevelopment of many muscles.

How do they age, they generally produce deformities called contractures multilateral, which limits the campaign for the joints. to restrict the abnormal muscle clumsiness, muscle weakness, and forced movements of the arms and legs too much mobility. In males (who have only one X chromosome), a transcription of the altered gene in each cabin is sufficient to induce the circumstances. With women (who have two X chromosomes), it will cause a variant in both copies of the gene, the existing disease. A spectacular feature of the X-linked inheritance is that fathers do not transmit X-linked traits to their son. A physical examination, medical history, and a number of tests can help diagnosis. Associated features often include underdevelopment and muscle wasting, weakness and stiffness in the legs with exaggerated reflexes, relatively slow, involuntary, purposeless, writhing movements (athetoid movements), and other movement abnormalities . Allan Herndon syndrome is considered X-linked recessive inheritance and is therefore regarded as a principle at all expressed in males only. There is no cure for the syndrome Allan Herndon Dudley Also there is no specific treatment. The treatment is very personal. Because patients are usually affected cognitive, special education and structured care is needed. Physical therapy seems to help with some mobility problems.

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