Essays on Trisomy

Genetic and genomic knowledge is a vital part of being a good nurse and meeting all of the competencies that are required to care for patients. There are a large number of genetic diseases, for example, and the field is extremely fast-paced. This makes keeping up-to-date with the information available important but challenging. It was an interesting process learning about all of the various elements of genetic information and how it can be used in nursing as well as generally assisting all health care professionals. The purpose of this paper is to discuss some of the information that I ...

Trisomy

Chromosomes are marvelous things! They carry in their genes the entire genetic code required to build a human being. Comprised of nucleic acid (DNA) and proteins, twenty-three pairs of chromosomes located in the cell nucleus are needed for the normal development of a human embryo. However, sometimes things go wrong. This paper will discuss some of the consequences of faulty chromosome separation during fertilization, resulting in Trisomy. Trisomy is a chromosomal condition which occurs when three chromosomes, instead of the normal two are produced during cell division. This happens due to the failure of human chromosome pairs to separate ...

DOWN’S SYNDROME

Describe a patient with the condition of Down’s syndrome. Answer: Julie, an eighteen years old female patient was diagnosed with Down’s syndrome. She was dependent on her parents for basic routine tasks like washing and dressing. These issues began to pose as more problematic day by day as it was not possible for her to go out on trips with her friends. She was unable to move out of her home due to her extreme dependency on her parents (Katemeadsassociates.com, 2016).

What is Down’s syndrome?

Answer: Down’s syndrome is a medical condition that develops as a result of Trisomy of ...

Vanishing Twin Syndrome

Vanishing Twin Syndrome In 1945, Walter Stoeckel proposed that the general population of conceptions were higher for multiple fetuses that supposed, suggesting that a twin or multiple fetuses may die in utero and subsequently be reabsorbed without clinical evidence by the surviving fetus/es, mother, or placenta (Stoeckel, 1945, cited in Levi, 1976). Named the “vanishing twin syndrome”, the cause is generally not known. If abnormalities are determined, they appear related to early development and are chromosomal; improper implantation of the cord may also play a role. This paper presents a brief overview of the etiology, demographics, consequences, and tests ...

Lis Rodriguez

Lab 1 ASA College Abstract Patau’s syndrome is a rare genetic disorder that involves trisomy 13. The condition is characterised by either an extra copy of the autosomal chromosome number 13 or a translocation to chromosome 13 from another chromosome. There are severe symptoms observed in the unborn and newborn children having this defect. Polydactyly, cleft lips, physical retardation, mental retardation, heart defects are few of the many symptoms. The disease can be diagnosed during gestation via screening methods followed by several analytical procedures like FISH, karyotyping and microarray on samples of blood and serum from the pregnant ...