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Genetic problems , down syndrome, hurlintong disease, diabetes, and turner syndrome - Research Paper Example

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Each specie has different DNA(deoxyribo-nucleic acid) molecules which encode the genes and different genes determine the different characteristics of the…
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Genetic problems , down syndrome, hurlintong disease, diabetes, and turner syndrome
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Download file to see previous pages Sometimes errors can occur in the transmission of genetic material from parents to offspring or in the structure of the genetic material causing serious disorders in human beings. Structural chromosomal abnormalities arise when different enzymes are not able to repair several breaks in the pattern of chromosomes or even if they are able to do so these repairs are not specific enough to avoid the abnormality. These can be caused by chemicals, radiations, viruses, or any other type of abnormal event. These structural abnormalities are classified into four main classes respectively. These are Deletions, Translocations, Inversions and Ring Chromosome (Langman & Sadler 2006; Robbins et al 2005).
Other names of deletion are gene deletion and deficiency mutation. Deletion is that type of genetic abnormality in which a sequence of DNA is absent in the chromosome or a part of chromosome is absent. It results in the loss of the genetic material from the chromosome. Translocation is also genetic aberration which occurs due to the rearrangement of the different parts of chromosome with nonhomologous chromosomes. Translocations are of two types that are reciprocal translocations and Robertsonian translocations. Reciprocal translocation is the translocation of genetic material between nonhomologous chromosome. These type of chromosomal translocations are harmless. When the two acrocentric chromosome fuse near the centromere resulting in loss of the short arm, this type of translocation is called Robertsonian translocation. In Robertsonian translocation the resulting karyotype in humans is 45 chromosomes. Inversion is that type of chromosomal abnormality in which a part of chromosome is split and introduced back to the same chromosome. Inversion is basically the aberration in a single chromosome itself and is not associated to other homologous or nonhomologous chromosome. Inversions are of two types paracentric and pericentric. ...Download file to see next pagesRead More
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Down Syndrome the medics. Moreover, it cannot be dispensed that a significant number of people have been victims of such genetic disorders. In particular, Down syndrome commonly referred to as Trisomy 21, and a genetic disorder, is a disease that has affected many people, and as research would have it, it remains the leading cause of cognitive impairment Genes (Hindley 42). Reportedly, the disease affects approximately one out of the eight hundred live births every year (Hindley 56). Conventionally, scientific innovations coupled with extensive research are the answers to such health problems human beings are made to experience....
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Down Syndrome understand this problem especially in regard to nursing management and available community resources. Introduction Down syndrome is a genetic disorder which results to lifelong pathophysiological problems including developmental delays and mental retardation. It is a condition in which an individual is born with an extra chromosome 21 copy (Dykens, 2007). Individuals suffering from this condition tend to have intellectual disabilities, as well as physical problem. Also, they may have other health problems such as dementia, heart disease, hearing problems, problems...
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