Hemophilia is a genetic disorder in which a person has an absence of blood clotting proteins/factors, causing their blood to clot abnormally (Bad Blood). Those with this disorder have a tendency to bleed for longer periods of time compared to people with normal clotting proteins/factors (Mayo Clinic).…
1. A 35-year-old male has come to see you because he is urinating, by his estimate, about 8L/day. He is constantly thirsty and drinks as much cold water as he can every day. His sleep is disrupted because of the need to urinate throughout the night. During your assessment, you learn he had several concussions playing college sports.…
One person could inherit the gene, but not get the blood disorder, but it could still be passed on to an offspring. The gene would probably appear in an inbred line. ”(Blue People Genealogy 7) Martin Fugate carried the gene and the odds that he could have married a woman with the same recessive gene which is what happened. But Cawein was able to find an antidote for the blood disorder.…
The reason why I choose this topic because it's a condition I have been dealing with when I was growing up and it had a big impact on my life. It effect me in many different ways where I would have to go to the hospital and some time the doctor wouldn't have a clue on what was happening to me? So one day my doctor Anna Marie had took the time to analyze my labs until she seen that I had a low count of white cells and it was very serious matter to take care of. At the time I didn’t understand what was going on with my body and why I was having bloody nose and even getting bruises all the time. Then my doctor told me that I had Idiopathic Thrombocytopenic Purpura.…
Von Willebrand Disease Von Willebrand disease is the most common bleeding disorder. It occurs when the body makes too little of the von Willebrand factor (VWF), a protein that helps blood clot, or when the VWF is misshapen and does not work the way it should. VWF is a carrier for another protein, called factor 8, that helps blood clot. When VWF levels are low or when VWF is not working properly, factor 8 levels are low as well and the body is less able to form stable blood clots.…
This is a disease in which the hemoglobin protein is produced incorrectly and the red blood cells have a sickle shape. A person that is homozygous recessive for the sickle cell trait will have sickled red blood cells that all have the incorrect hemoglobin. A person who is homozygous dominant will have normal red blood cells. From the images on the first page in the packet, this trait is an example of incomplete dominance, as a person who is heterozygous for the sickle cell trait will have some misshapen cells and some normal cells. From the results, this was the case for the…
Carbon monoxide poisoning is fatal. Carbon monoxide binds to haemoglobin at the same site as oxygen – the iron atom within the haem group – however carbon monoxide will bind with a strength 200 times that of oxygen. This means that if carbon monoxide is inhaled it was always displace oxygen within haemoglobin. If oxygen can no longer bind to haemoglobin then the respiring cells of the body can no longer receive oxygen and will eventually die. When carbon monoxide binds to haemoglobin it causes the haemoglobin to shift from the T form to the R form, so oxygen quickly binds to the other available haem groups within the haemoglobin.…
Birt-Hogg-Dubé syndrome also known as BHD is a hereditary disease first described in 1977. Name of the disease came after last name of the three Canadian doctors that found the disease, Arthur R. Birt, Georgina R. Hogg, and William J. Dubé. The BHD was discovered in 1977 association with the skin lesions, but the connection with the lungs and the kidneys were not found until 2002. BHD is an autosomal dominant genetic disorder that primarily affects the skin, lungs, and kidneys. Autosomal dominant disorder means an abnormal gene that cause the disease is passed down from one parent, and men and women are likely to be equally affected, which means each offspring has a 50% chance of having the disease.…
The disease is genetically inherited and is a recessive. To be exhibited in…
According to “Essentials of Pathophysiology” by Carol Porth, “sickle cell disease is an inherited disorder in which abnormal hemoglobin (hemoglobin S [HbS]) leads to chronic hemolytic anemia, pain, and organ failure”. The recessive gene is inherited and appears as the sickle cell trait if heterozygous or sickle cell disease if homozygous with two HbS genes. The amount of hemoglobin that is affected by the gene depends on if they are heterozygous or homozygous, and therefore affects the gravity of the symptoms (Porth, 2014). “Approximately 8% of African Americans are heterozygous for HbS and 0.1% to 0.2% are homozygous” (Porth, 2014, pg 283), and according to the Central of Disease Control, 1 in 365 Black or African-Americans and 1 in 16,300…
And then that gene gets other genes to get involved into the development. The parents do not pass this disease down but rather the mutation happens in the own girls body. But the mutation that causes this disease occurs randomly. But scientist are still trying to find…
Sickle Cell Anemia is a blood disorder that causes red blood cells to become misshapen and not live as long as a regular blood cell. This sickness is a genetic…
Hemophilia Hemophilia is a rare hereditary bleeding disorder where the blood cannot clot normally at the site of a wound or injury. Where someone who has a minor cut can profusely bleed, and it can get so bad that it could end up making them sick. There are two types of hemophilia, Type A and Type B. Type A: Is the most common type, it is caused by lacking Factor VII, which is one of the proteins to help blood form clots. Type B is caused by lacking Factor IX.…
Hemophilia A and B is a bleeding disorders, congenital where the adults and children can have blood clot inherited condition. Children with hemophilia condition, have a bleeding problem and do not stop bleeding as quick as other children. For people who does not have hemophilia, a little, small cut its not a such big problem but, people who suffers from hemophilia, this little cut is deep bleeding inside their body. Especially it affects their knees, ankle, and elbows. In many occasion people with this internal bleeding can damage their organs and tissues, also it could be life-threatening.…
Hemoglobin job is to allow red blood cells to carry oxygen throughout the body. Abnormal hemoglobin causes the red blood cell to become rigid, sticky, and misshapen. The sickle cell gene can be referred to as Autosomal recessive inheritance, because it is passed down through generations in a pattern of inheritance. A child can be affected by sickle cell is the mother and father passes down a defective gene. If only one parent passes the sickle cell gene the child will have the trait; sickle cell trait produces both normal and sickle cell hemoglobin.…