Tecage General Discussion Pernicious anemia is a rare blood disorder characterized by the inability of the body to properly utilize vitamin B12, which is essential for the development of red blood cells. Merck Research Laboratories; Years Anemiw,, Genetic diseases are determined by the combination of genes for a particular trait that are on the chromosomes received from the father and the mother. Megaloblastic anemia Megaloblastic anemia is a rare blood disorder characterized by the presence of abnormal white blood cells, low white blood cell counts, and abnormally low levels of circulating platelets. Pairs of human chromosomes are numbered from 1 through 22 and the sex chromosomes are designated X and Y.
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Maugrel This disorder occurs much more frequently among people who have diseases such as multiple myeloma and various other immunoglobulin deficiencies than in the general population. The numbered bands specify the location of the thousands of genes that are present on each chromosome. Affected infants may experience repeated episodes of extreme anemia and jaundice. People with pernicious anemia must continue to receive maintenance doses of vitamin B12 throughout life.
In acquired aplastic anemia, an almost complete absence of hematopoietic stem cells ajemia results in low levels of red and white blood cells and platelets pancytopenia. Recurring episodes of anemia megaloblastic and an abnormal yellow coloration of the skin jaundice are also common.
Pernicious anemia is more common among people from northern Europe, Scandinavia, and North America than among those from other parts of the world. Genetic counseling may be of benefit for people with pernicious anemia and their families. Recessive genetic disorders occur when an individual inherits the same abnormal gene for the same trait from each parent.
Some people with pernicious anemia may also become extremely irritable or depressed and, in some rare cases, even experience paranoia megaloblastic madness.
Vitamin B12 deficiency is characterized by abnormally low levels of circulating B12 due to a poor diet or inadequate absorption of this vitamin by the stomach. Some children with the juvenile form of the disease have blood protein present in their urine persistent proteinuria and some may have urinary tract malformations.
Pernicious anemia is thought to be an autoimmune disorder, and certain people may have a genetic predisposition to this disorder. Bone marrow is the spongy substance found in the center of the long bones of the body.
Symptoms of pernicious anemia may include fatigue, shortness of breath, rapid heart rate, jaundice or pallor, tingling and numbness of hands and feet, loss of appetite, diarrhea, unsteadiness when walking, bleeding gums, impaired sense of smell, and confusion. The Juenil Manual-Home Edition. The myelodysplastic syndromes are a group of diseases that affect bone marrow. Pernicious anemia is thought to be an autoimmune disease. Most affected infants develop a form of anemia known as megaloblastic anemia.
The diagnosis of pernicious anemia may be confirmed by a thorough clinical evaluation, including a detailed patient history and specialized laboratory tests. Myelodysplastic syndromes The myelodysplastic syndromes are a group of diseases that affect bone marrow. A genetic polymorphism in the coding region of the gastric intrinsic factor gene GIF is associated with congenital intrinsic factor deficiency.
Rare Disease Database If an individual receives one normal gene and one gene for the disease, the person will be a carrier for the disease, but usually will not show symptoms. Cecil Textbook of Medicine.
When the disease goes undiagnosed and untreated for a long period of time, it may lead to neurological complications. Healthy bone marrow produces immature blood pernicipsa that then develop into red blood cells, white blood cells, and platelets.
Years Published,, Nerve cells and blood cells need vitamin B12 to function properly. The vitamin is labeled with radioactive cobalt and is ingested by mouth.
There is a rare congenital form of pernicious anemia in which babies are born lacking the ability to produce pernkciosa intrinsic factor.
Alone we are rare. Nerves other than those of the brain and spinal cord peripheral nervous system are frequently affected. All studies receiving Juvenio. University of Maryland Medical Center. X-ray studies can then determine if the body is properly absorbing this vitamin.
Pairs of human chromosomes are numbered from 1 through 22 and the sex chromosomes are designated X and Y. Chromosomes, which are present in the nucleus of human cells, carry the genetic information for each individual. Unlike pernicious anemia, people with Vitamin B12 deficiency typically have normal levels of intrinsic factor. Information on current clinical trials is posted on the Internet at www.
The Merck Manual, 17th anemoa. The risk is the same for males and females. All individuals carry a few abnormal genes. The gene responsible for anemia due to perniciossa intestinal malabsorption of vitamin B12 has been tracked to sites on chromosome 14 14q32 and 10 10p There is also a juvenile form of the disease, but pernicious anemia typically does not appear before the age of Males have one X and one Y chromosome and females have two X chromosomes.
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