Cell disease

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    Sickle Cell Disease (SCD) is a group of red blood cell disorders characterized by the presence of the Sickle Cell Trait (Center for Disease Control5 [CDC]). This genetic disorder affects erythrocytes, red blood cells, causing them to form in a sickle or “C” shape. Not only does this abnormal change in shape cause a shortage of red blood cells, they also continuously create a shortage of oxygen to each and every cell. Though the sickle cell trait is most commonly found in geographic locations where

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    Sickle-cell disease Chenglie Nanjie Sickle cell disease is a kind of disease that contains a group of disorders that affects hemoglobin, the oxygen-carrying molecule in red blood cells that transfers oxygen to cells (U.S. NIH, 2012). A particular mutation in the HBB (hemoglobin, beta) gene causes sickle cell anemia, a common form of sickle cell disease (U.S. NIH, 2014). Sickle cell disease can lead to various symptoms. Most significantly, it leads to very acute and chronic pain as well as organ

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    silent killer of children is sickle cell disease. This autosomal recessive disorder is multisystemic and commonly accompanied by acute illness episodes and progressive organ damage.27 Commonly fatal,8 it is considered one of the most “common severe monogenic disorders in the world.”27 Sickle cell disease describes a group of genetic conditions that are the product of either homozygous inheritance of the sickle cell gene or heterozygous inheritance of the sickle cell gene with another gene. 29 There

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    The focal point of this journal article focused on how the inherited genetic disease; Sickle cell anemia, is influenced by ethnicity and ancestry; two key categories that must be considered when explaining genetic associations and comparing traits amongst a population. This article compared the genetic profiles of African Americans with sickle cell disease to individuals of the Caucasian/ European descent and African descent. They discovered that although there is slight genetic comparison between

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    What is sickle cell disease? Sickle cell diseases are inherited blood disorders that affect mostly African Americans about 70,000 people in the United States. The studies shows approximately 2 million Americans have the sickle cell trait. The sickle cell trait occurs in about 1 in 12 African Americans and sickle cell disease affects millions of people worldwide. The rate for sickle cell disease or sickle cell trait is higher in people who live in Africa, South or Central America, the Caribbean islands

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    Sickle Cell Disease wasn’t discovered until 1910 in the United States making it’s 100th anniversary in 2010. Since the discovery, many people have been affected by it. People can either carry the disease or the trait. When a person carries the disease, they have all the symptoms of sickle cell. When a person carries the trait they are not affected by the symptoms but will pass the gene down to their offspring. What is Sickle Cell? The Sickle Cell Disease is a group of inherited red blood cell disorders

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    Sickle Cell Disease Sickle cell disease is a hereditary blood disorder caused by an abnormal hemoglobin in the red blood cell. Hemoglobin is a type of protein that carries oxygen in the body. In order for someone to have sickle cell disease they would need to have been passed down from at each one of their parents, by inheriting a total of two hemoglobin genes. The fact that this is a hereditary disease means that it is not considered to be contagious. This disease comes in about six different forms

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    Jack Gardner Honors Biology Organelle Disease Essay 7th Hour Sickle Cell Disease Sickle cell disease (SCD) is a hereditary blood disorder that occurs due to an abnormality in the oxygen-carrying protein hemoglobin found in red blood cells which causes the sickle hemoglobin (HbS) to polymerize and form a sickle or a crescent shape instead of the circular shape of healthy red blood cells (Sickle Cell Disease, George). Ribosomes are responsible for the creation of protein in the body, meaning it is

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    degenerative disease experienced at a higher rate among Black/African Americans (vs. American majority statistics) A degenerative disease experienced at higher rate among Black/ African Americans is sickle cell disease according to the Journal of Bioprocessing & Biotechniques. It happens at a higher rate in African Americans or those of African descent than any other group. Sickle cell disease is a severe hereditary form of anemia that and have abnormal haemoglobin which distorts the red blood cells. 1 in

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    diagnosis and explain why. 1) Sickle Cell Disease (SCD) (Sickle Cell Crisis): Sickle cell disease is a hereditary disease. The majority of individuals affected by SCD are those of African descent (Yawn & John-Sowah, 2015). SCD develops hereditarily by an individual being homozygous for sickle hemoglobin (HbSS) (Yawn & John-Sowah, 2015). Individuals will also have another abnormal hemoglobin gene, such as HbSC (Yawn & John-Sowah, 2015). The red blood cells (RBCs) in SCD lose oxygen and become sickled

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