Cystic Fibrosis is a common and inherited disorder of the respiratory system. A mutation of the cystic fibrosis transmembrane regulator gene causes cystic fibrosis. This gene is located on chromosome seven, and this chromosome manages a chloride channel found in the tissues of the exocrine. If the channel is blocked, then thick secretion will build up in the lungs, and other organs and it will be extremely hard to eliminate. This can lead to severe issues, or even death. This study gathered information about the cystic fibrosis mortality rate from infants and children in Spain. The purpose of this study was to find out how many infants or children had passed away because of cystic fibrosis. This information then assisted in the development …show more content…
It can affect anyone, but mostly children. Children who have cystic fibrosis are at great risk. According to the study, children under age one have the highest mortality rate. It is unknown why, but according to the study it has improved greatly because of new treatments that are being created. This article was informative and it read easily. The language was simple and easy to understand. I enjoyed the background information about cystic fibrosis at the beginning of the article because it informed the reader of what was about to be discussed. Also, I was intrigued by all of the data that was presented in this article, I enjoyed learning about who the disorder had affected. However, the excess data took the focus away from infants and children and spoke about people with the disorder as a whole. It was a little confusing to me because I felt like the results were not that accurate because adults were included in the study. However, there is enough sufficient data to support that children have a higher mortality rate due to cystic fibrosis; it is clearly stated in the results as well as in the data. Further studies can be improved by focusing the study on one specific age group, instead of multiple. The question that remains unanswered in this article is why do children have such a high mortality rate due to cystic fibrosis. Now that I know children have a higher rate, I would like to know why. Overall the article was
Congestive Cardiac Failure Keywords: Congenital, heart disease, cyanosis, oxygenated blood, deoxygenated blood, structural defects, systemic circulation, pulmonary circulation, Mottling, Pallor, Pulmonary Rales 1. CYANOTIC CONGENITAL HEART DISEASES (CCHD) CCHD is a group of congenital heart diseases that occur due to deoxygenated blood bypassing the lungs and entering the systemic circulation or a mixture of oxygenated and deoxygenated blood entering systemic circulation which is caused by structural defects of the heart or any condition which increases pulmonary vascular
A case is presented at the hospital of a 2-month-old child, diagnosed with down syndrome, and currently recovering from a case of bronchiolitis. The child, Elisa, is also diagnosed with Tetralogy of Fallot, and she will undergo surgery to correct this defect once she has had time to recover from her bronchiolitis. Elisa is the sixth child or Maria and Hector. She has three brothers and two sisters who range in age from 10 to 25 years old.
The parents need to get their child or children vaccinated to prevent the spread of the disease. Children can easily be affected because of germs and it can also spread
The only major problem with the article is being outdated but most of the information and findings are relevant
Although overall the subject was interesting, the method in which it was written seems to be sloppy and rush. At this juncture, I will explain the details in which drives me into believing such things about a published article. When writing a paper it is common practice to
Discovered in 1989, Cystic Fibrosis is the most common, fatal genetic disease in the United States. Statistics show that 30,000 people in the US have been named with this disease. (Genome) Cystic Fibrosis is a disease caused when the CFTR (Cystic Fibrosis Transmembrane Regulator) is defective and the cells do not release the right amount of chloride. This causes for the body to produce thick, sticky mucus that clogs up the lungs, leads to infection, blocks the pancreas, which stops the digestive enzymes from reaching the intestine. Symptoms require; salty tasting skin, wheezing, shortness of breath, persistent coughing, poor growth or weight gain, frequent/bulky stool, and male infertility.
In my childhood I rarely took notice to the impact that Cystic Fibrosis was leaving on my life. But, by my adolescent years it became almost impossible to ignore that having CF made me unlike my peers. While having CF did have many negative impacts on my life as any life-threatening condition does, I believe that my CF molded me into a strong, independent, intelligent young woman. Compared to many of my peers I find myself to be more ambitious and dedicated to my goals. People have often told me that I am hard on myself when it comes to dreams and goals.
Cystic Fibrosis is caused by a mutated gene that changes the protein that controls the salt in and out of the cell. There are many different mutation which can change the severity of the disease in each case. For this to be passed on a child must receive one copy of the gene from each parent to develop this disease. If a child receives a copy from only one parent then
This document will analyse the serious case review of an 8 year old child. Following confidentiality protocols the child will be referred to as Child H. This case was reported to the Bury safeguarding board when the child died of an asthma attack in April 2013 following ...... give dates and reference. . Child H had two siblings one older brother who was ten years old and a younger sister aged five years old at the time of the incident. Child H and his family had a number of issues raised by individual agencies and (to the Bury Safeguarding Children Board (BSCB), for families with risk factors, multiple needs or complex within the families. ??????? give more details later about the plan of the
Overall, the article was fairly decent. It was not very easy to follow, as state before; I had to research outside of the article for more clarification on certain words and procedures. The information used was quite old as well. The article was written in 2012 and majority of the information was from the early to late 90’s. One chart that would have been very useful if it was up to date contained information from 1995.
I feel like the conclusion was well written and ended the article in an appropriate way. It might not be the way I would have written it, but I think their effort to help people understand that they need to take care of themselves, is
If a child has asthma this can affect them because they might not be able to run around as much as their friends. This may affect their physical development is some areas as they can’t be as active and can’t take part in physical activities, and it might affect their social development because they can’t run around with their friends. Another personal factor is learning difficulties. If a child has learning difficulties then they will need extra support with some areas.
Overall I believe this document is very healthy and helpful for the readers who just want to know about the
Parents and family members with a child of any age would also benefit from the information delivered in this speech although older children may not receive such impactful results. Significance: This speech is relevant to my audience because the impact of such a significant diagnosis is a life changing and emotional event for families and the need for direction and guidance at such a critical time in their child’s life is essential. My audience should understand that providing their child with early intervention therapy will impact their child’s life indefinitely.
Cystic Fibrosis is a hereditary condition, and for a child to get the disease, they have to get one copy of the defective gene from their mother and their