Children With Down Syndrome

There is no regular treatment for Down syndrome, the treatment is different for everyone depending on the physical and mental barriers they have. Someone with Down syndrome will most likely seek help from specialists, speech therapists and other people to help with the mental and physical needs of the person. People with Down syndrome are more adept to illnesses or conditions so it is necessary for them to be checked on by a doctor, etc. more often.

. Down syndrome is not a disease that someone catches and is not caused by difficulties during the pregnancy, it is a genetic condition. This condition is caused by the presence of an extra chromosome in the body’s cells and causes a redundant amount of proteins to be formed. All cells of the body derive from a single cell formed by the fusion of a father’s sperm and a mother’s egg. Each cell carries a nucleus full of genetic material known as genes. These genes are inherited from both the mother and father. Each cell normally contains 46 pairs of chromosomes. 23 chromosomes come from one parent and 23 from the other, hence the 46 pairs. When it comes to children with down syndrome, one of the chromosomes does not separate properly and so the

There is no single, standard treatment for Down syndrome. Treatments are based on each person's personal needs, limitations, and strengths. A child with Down syndrome would likely receive care from a team of health professionals, which includes physicians, special educators, speech therapists, occupational therapists, physical therapists, and social workers. “Early intervention” refers to a range of specialized programs and resources that professionals provide to children with Down syndrome as well as their families. A variety of therapies can be used in early intervention programs to promote the greatest possible development, independence, and productivity. Some of these therapies include physical therapy, speech-language therapy, occupational

Also known as Trisomy 21, Down Syndrome is an illness due to which an superfluous genetic structure leads to delays in the manner in which a child’s mental and physical faculties develop.

Down Syndrome is also known as Trisomy 21, is a disorder that occurs when an extra chromosome is present on the 21st chromosome. There

Down Syndrome is a genetic disorder that occurs when a persons 46 chromosomes abnormally divides into 47 chromosomes, creating a full or partial 3rd copy of the chromosome 21.

Down syndrome is a genetic defect attributed to an abnormality of the human chromosome 21. The National Down Syndrome Society (NDSS), a national advocate organization for the value, acceptance and inclusion of people with Down syndrome, notes that modern research has successfully identified three types of Down syndrome. The NDSS reports that Nondisjunction Trisomy 21, in which there are three copies of chromosome 21 instead of two, is the most common type of Down syndrome. Prior to or at the point of conception, a pair of 21st chromosomes in either the

Down syndrome is commonly known by the public as a disease that causes physical and mental disabilities in people. Down syndrome is known by the scientific community as a genetic disorder of the twenty-first chromosome. As a result of this genetic disorder other systems of the body are also affected, this includes mental and physical disabilities. Down syndrome “is a lifelong condition… that happens before birth” (WebMD, 2015). According to the National Down Syndrome Society one in every 691 babies are born with the condition (NDSS, 2015). In order to understand this condition it is

The genetic cause of down syndrome is when people have 47 chromosomes in each cell instead of 46, which is what most people are born with. Down syndrome, also known as Trisomy 21, is a genetic disorder associated with an extra chromosome 21. Trisomy 21 is caused by an error in cell division, which leaves a reproductive cell with an extra copy of chromosome 21. The

The article “Down Syndrome” reviewed by Dr. Mary Gavin, thoroughly explains the causes, affects and diagnosis of the condition. This genetic condition involves the individual gaining an extra chromosome, ending up with 47 instead of 46. A person with Down syndrome facial and bodily features will be distinctly unique, making it easy to characterize them from others. Consistent medical attention is crucial for a child with the condition, even if the child appears to have no significant health concerns. With out proper care, the child could develop pulmonary hypertension, worsened vision and hearing, seizures, asthma, infections etc. Prenatal screening

Down Syndrome has lots of complications as stated before individuals can have intrinsic heart problems, respiratory problems and listening to the issues, Alzheimer's disease, adolescence leukemia, and thyroid conditions. There is no cure for Down Syndrome, but the goals are to control the symptoms and the resulting medical conditions. As stated by Arthur Schoenstadt, MD “this includes regular checkups and screenings, medications, and surgery. Counseling and support groups are also aspects of treatment for those who need help in coping with the emotional and practical aspects of Down syndrome (Schoenstadt, 2013).

Down syndrome (trisomy 21) is a chromosomal abnormality - change in the number of chromosomes, which lead to physical or mental abnormalities - caused by an error in cell division that is a result of having an extra 21st chromosome. 95% of the time the trisomy is mainly due to an abnormality of the egg of a mother, during fertilisation the 23 chromosomes from

Every person with Down Syndrome is different. Both developmental and intellectual problems can go from mild to moderate. Some individuals can be completely healthy, whereas others can suffer from serious health issues such as heart defects. Not every child with Down Syndrome has the same characteristics although some are more common than others such as a distinct facial appearance. ("Down syndrome Symptoms - Mayo Clinic",

Down syndrome is characterized as a chronic genetic chromosomal disorder which alters one’s cognitive growth, intellectual development, and physical characteristics. This extremely widespread condition is most prominently existent in human beings whose genetic makeup is composed of an additional copy of chromosome 21. Additionally, these human beings are known for acquiring 47 chromosomes rather than the conventional 46 chromosomes. This chromosomal abnormality is extremely common, yet highly spontaneous. To illustrate, the prevalence of Down Syndrome is exhibited as around

There are three forms of Down Syndrome. These three are Trisomy 21, Mosaicism, and Translocation. Trisomy 21 is where there is an extra copy of Chromosome 21 in every cell. Mosaicism is where only some of the child’s cells have an extra copy of Chromosome 21. Translocation is where only one of the 46 total chromosomes has an extra Chromosome 21 where part of Chromosome 21 gets attacked to another chromosome during the formation eggs and sperm, or early in the development of the fetus. Mosaicism and Translocation usually have less symptoms that Trisomy 21. Only translocation Down Syndrome can be inherited by an unaffected parent. Trisomy 21 is because of an abnormality in the reproductive cells, and mosaic Down Syndrome is just a random event that occurs early in fetal development. A baby receives 23 chromosomes from each parent, but with a Down Syndrome child, they receive extra chromosomes. When the Chromosome 21 is supposed to split into two chromosomes, the chromosome does not separate properly and they get three Chromosome 21. So as the brain and physical features develop, problems occur. Down Syndrome affects 1 in 800 newborns. Each year in the United States, 5,300 babies with Down Syndrome are born, and 250,000 people have this condition in