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Translocated Down Syndrome Translocated Down Syndrome is genetically passed on from a parent gene to its own child (tubal Crucial, 2012). In this paper we'll look at a brief description of the Down syndrome really is, the genetic causes of Translocated Down syndrome, symptoms, characteristics, drugs, intervention plans and testing to Down syndrome while an infant remains in the womb. The effects of Down syndrome are brought on by an extra chromosome. "a genetic disorder, associated with the existence of an excess chromosome 21" (Dictionary.com, 2014). Individuals with Down syndrome have another appearance for them, as their eyes are usually slanted, they are far shorter, whether their parents are tall or not and their tongue/mouth isn't structured the same as everyone else's (WebMD, 2014). These are many of the characteristics of Down syndrome. Translocated is the only genetic cause of Down syndrome proven to be passed along through a parent's receptor. The parent may be the carrier of the flaw or it may be an unsuspected trait (Clinical Key, 2012). Translocated is a rare cause, but it's definitely not impossible. What happens is chromosome 21 links itself into other chromosomes. This occurs past to conception or it can happen during. People with translocated still have the normal chromosome 21, but they've got extra things from chromosome 21 added onto the translocated chromosome (Mayo Clinic, 2014). Translocated is another kind of Down syndrome, using the distinction of it being passed along with genetics. There are two distinct sorts of symptoms: You'll find intellectual and physical symptoms. Some of the physical symptoms are a smaller neck, eyes are slanted up, and hands are wider than regular and also both their hands and finge...