Genetic Diseases Essay

a medical condition in which a thick and sticky mucus progressively covers organs, causing them to malfunction. This disease is commonly known for affecting the lungs and bronchi, however there are many more risks the disease brings to organs. Not only does Cystic Fibrosis bring risk to organs, it runs risks to all people. Everyone carries two CFTS genes, however the genetic disease only occurs hereditarily in offspring of two carriers holding damaged CFTS genes. Cystic fibrosis brings a fragile lifestyle

Childhood diseases can be some of the most exhausting, stressful, and difficult situations that a family has to go through. It can affect them physically, emotionally, spiritually, and psychosocially. Sick children are more likely to have genetic diseases rather than environmental diseases due to the fact that they are young, and have been exposed to less harmful situations and organisms (Ament, 2003). Unfortunately, many times genetic diseases are fatal, debilitating, and incurable. One of these

A.Who first discovered the genetic disorder or autoimmune disease? Kraepelin recognized biological causes of mental illnesses. He is believed to be the first person to seriously study mental illnesses. Kraepelin 's Manic Depressive Insanity and Paranoia in 1921 detailed the difference between manic-depressive and praecox, which is now known as schizophrenia. B. Is the disease state recessive or dominant? One study has also found a higher frequency in families where the disorder is inherited from

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.

Currently, stem cells are used to treat a few diseases, including the Stargardt’s macular dystrophy and leukemia. Stargardt’s disease is a genetic disease that may lead to the loss of vision. This is due to the degeneration of photoreceptive cells, the component in the retina of the eye that detects light. This disease is a result of a recessive mutation of a gene named ABCA4, which leads to the malfunction of membrane proteins that are responsible for the active transport in retina cells. By using

but is curious about why cancer is a genetic disease. She has tried to understand what the doctors are saying and has even done some research herself but remains confused. Below is the conversation. Nurse: Good afternoon Mrs. Jones. I know earlier you were hoping to sit down and discuss why cancer is a genetic disease. I have some time now if you would like to discuss it? Mrs. Jones- Why yes that would be excellent. You know I am ready to tackle the disease but still have a lot of questions especially

diagnosed with Parkinson’s Disease in his late 60’s, and his body progressively deteriorated until he passed away. This is just one of the many Parkinson’s disease cases reported each year; although medications and treatments are given out, they can only relieve related

Down Syndrome, also known a Trisomy 21, is the most common cause of Mental deficiency that occurs from childbirth. Down syndrome is a genetic disorder that occurs when there is an extra chromosome Present. The presence of an extra chromosome causes this genetic disorder because chromosomes contain all of our genetic information and when this information is disrupted during cell division for example, when one is conceived with an added chromosome this causes many problems with the coding of the DNA

In 1938, Dr. Henry Turner first described Turner Syndrome. Turner Syndrome a genetic disease that only affects girls, in fact, it is one of the most common sexual development disorders (Radtke et al. 2014). It is caused by an abnormal sex chromosome, either an abnormal X chromosome or a missing X chromosome. The sex chromosome contributed by the father to the child determines the sex of the child because the mother always contributes an X chromosome whereas the father can contribute either an X chromosome

threatening disease, that as of now has no cure. But with help from extensive research that is being conducted, there is soon to be a cure in the future for this disease. The disease attacks the digestive system and slowly over time shuts down the lungs. Cystic fibrosis is a genetic disease that is passed down from the parents to the children. Some parents may not know they are carriers of this disease, there is a 1 in 50% chance that people can be a carrier of CF and not even know it. The disease can