Down Syndrome Essay

child, or do have a child with Down syndrome, it is a life changing experience that most need guidance with. 1. The Center for Disease Control and Prevention state that, “Down syndrome continues to be the most common chromosomal disorder. Each year, about 6,000 babies are born with Down syndrome, which is about 1 in every 700 babies born.” 2. Heart Problems: The Center for Disease Control and Prevention also state, “About 50% of all babies born with Down syndrome are also born with a congenital

doctor may bring a catastrophic change to this pleasure. You’ve blessed with a Down syndrome baby. Everything of your remote site seems to be gloomy. But don’t be upset. Come forward with the affection of fatherhood or motherhood and say- THOU BE MY HEAVEN, LITTLE ANGEL. Down syndrome Down syndrome is a set of physical and mental traits caused by a gene problem that happens before birth. Children who have Down syndrome tend to have certain features, such as a flat face and a short neck. They also

Is your child having trouble learning to speak, read, or walk? If so, you may want to get a screening test and a diagnostic test to see if your child has down syndrome. Down syndrome is a disease in which chromosome 21 has extra genetic material delaying the way a child develops mentally and physically. This means that babies with down syndrome have an extra chromosome, chromosome 47. Some symptoms of the disorder is physical features such as, flat facial profile, upward slant to eyes, small ears

older women as they occur within the half of the first trimester due to genetic problems including Down syndrome; as 1 in 53 at the age of 40 have a baby with a genetic disorder, compared to 1 in 1064 at 25 (Evidence Based Birth 2017). The increased risk of Down syndrome in 40 year old women is believed to be caused by errors which can crop up in the eggs’ genetic material as they age (Down-Syndrome Screening: A One-parent test for a Two-parent; The Atlantic 2017). Normally, there are 46 chromosomes

Down Syndrome, also known as trisomy 21, is a genetic disorder caused when there is three copies of the genes on chromosome 21 rather than two. This is a common disorder that affects many people. About one in every 691 babies is born with Down Syndrome in the United States. That means about 6,000 babies are born with Down Syndrome every year. This disorder causes many harmful effects that interfere with daily life. It can’t be cured, but treatment is available in many different ways.

Down syndrome is a genetic disorder that is common by birth defect due to having an extra chromosome of 21. Down syndrome causes delay in their development and some level of learning difficulty and has a characteristic facial appearance, and speech complexity. The aim of a person having Down syndrome is to help manage their lifestyles. However managing a person with Down syndrome lifestyle and living to the fullest is absolutely challenging, it will take time, hard work and financial means to make

Achieving satisfactory oral health outcomes has long been a barrier for intellectually impaired patients with higher incidences of oral diseases (Al Habashneh, Al-Jundi, Khader, & Nofel, 2012). Sandra is a 12-year-old, down syndrome patient who presents to the AIH clinic for a dental examination. It is evident Sandra consumes high volumes of sugary foods and beverages. Additionally Sandra has poor homecare resulting in neglected oral health. To address Sandra's oral health it is important to provide

with Down syndrome, how do you know that the person has Down syndrome? It is because of how they look. It is very easy for doctors and even the general public to notice that someone has this disorder. People with Down syndrome have slanted eyes, a flattened face, a big spatial difference between the eyes, and so on. Humans are used to seeing a basic facial configuration, so if an individual does not have a basic facial configuration but does have the characteristics of someone who has Down syndrome

Down syndrome (DS) caused by trisomy 21 is the most common human aneuploidy and occurs approximately in 1 in 700 live births. Individuals diagnosed with DS display a wide range of clinical phenotypes including cognitive impairment, mental retardation, craniofacial abnormalities as well as increased risks for congenital heart defects, gastrointestinal tract abnormalities including Hirshsprung’s disease, with the presence or absence and severity of these features varying amongst the individuals. Proper

Down syndrome as a cognitive disorder Down syndrome (DS) is relatively well known as a genetic disorder to the general public and children with this syndrome form one of the most readily identifiable groups of children with moderate to severe learning difficulties. It has been over 130 years since Langdon Down first described DS and 30 years since the presence of the defining extra copy of chromosome 21 was identified by Lejeune and his team of French geneticists. Delay