Geometry.Net - Health_Conditions: Aplastic Anemia

Aplastic Anemia - MayoClinic.com
aplastic anemia occurs when your bone marrow stops producing new blood cells. It s a serious problem, but treatments are available for this rare blood
http://www.mayoclinic.com/invoke.cfm?id=DS00322
News - Measurement Of Telomere Length Can Diagnose Dyskeratosis
Measurement of Telomere Length Can Diagnose Dyskeratosis Congenita, a Form of aplastic anemia
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Aplastic Anemia & MDS International Foundation, Inc. - Serving Patients With Apl
aplastic anemia MDS (Myelodysplastic Syndromes) International Foundation, Inc. serves as a resource directory for patient assistance and emotional support
http://www.aplastic.org/diseases.shtml

Extractions: The is the only organization in the world maintaining a voluntary Patient Registry to keep track of aplastic anemia, MDS and PNH patients for statistical analysis. Because these are not reportable diseases, statistics are not available to assist research and medical studies. Patients or family members may complete the Patient Registry Questionnaire online or download a print version and postal mail the form to us. Learn more about aplastic anemia, MDS and PNH. Read recent news items. Find out about clinical studies for aplastic anemia, MDS or PNH patients. In the United States, thousands of men, women and children are stricken with these non-contagious bone marrow diseases every year. They occur when the bone marrow stops making enough healthy blood cells. Although all of the causes are still unknown, they have been linked to toxins and viruses that we are in contact with every day. APLASTIC ANEMIA MDS PNH Aplastic anemia can be traced as far back as 1888 when a famous German pathologist, Dr. Paul Ehrlich, studied the case of a pregnant woman who died of bone marrow failure. It wasn't until 1904 that this disorder was termed aplastic anemia. Aplastic anemia occurs when the bone marrow stops making enough blood cells. The bone marrow is almost empty of blood forming cells and is described as
Having Patience When You Are The Patient!
A positive survival story.
http://www.geocities.com/hotsprings/villa/4803

Extractions: My name is Shari and I am an Aplastic Anemia Survivor. I am just beginning to build this page, so please be patient! In the mean time, please feel free to e-mail me at MIRACL2100@aol.com Thank you! SOMETHING ABOUT ME!!! I am a 33 year old female in remission with Aplastic Anemia. I was diagnosed in November of 1985. I was treated with over 200 blood transfusions(red cells and platelets), prednisone(steroids), ATG(Anti-Thymocyte Globulin), then, eventually had a splenectomy(removal of the spleen) in September of 1986. I was told I was in remission in the Spring of 1987. I can't ever be told that I'm cured, because, I have never had a bone marrow transplant. A bone marrow transplant is the only known CURE. Unfortunately, a perfect match could not be found for me. When I was diagnosed, my white count didn't exist at all. My hemoglobin was 4.0, and my platelet count was only 500(normal is 150,000-350,000). Therefore, my immune system was "shot". I was open to get all kinds of infections. I was bruised all over, had terrible migraines, and low blood pressure. The doctors even had to stop my menstrual cycle so I wouldn't bleed the little blood that I had left. You may be thinking, well, what's the miracle!! Well, that was all of the negative information. Now, for the positive: I've been in remission for 10 years now; I went on to finish college(I was a junior when I got sick), and, I got married. I didn't know if I'd make it through the Aplastic Anemia, and, not only have I survived the illness, I brought a new life into this world! On March 3, 1995, I delivered a healthy beautiful girl named Alexa. Her middle name is Faythe(for all the faith I had to get through the illness). I had the child that I never thought I could have, due to all of the medications I had taken.
The Aplastic Anaemia Trust
Charity dedicated to research into aplastic anaemia or bone marrow failure. Information on the disease and support group.
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Aplastic Anemia & MDS (Myelodysplastic Syndromes) International Foundation, Inc.
aplastic anemia MDS (Myelodysplastic Syndromes) International Foundation, Inc. serves as a resource directory for patient assistance and emotional support
http://www.aplastic.org/edmat_ty.shtml
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The aplastic anemia and Myelodysplasia Association of Canada s website has moved. Please update your bookmarks to www.aamac.ca
http://www.aamac.ualberta.ca/
Ilir's Progress With Aplastic Anemia
Includes information about aplastic anemia and Ilir's progress with this disease.
http://www.geocities.com/ilir_status/

Extractions: Recent Pictures. New!!! This page was last updated on: July 5, 2001 Ilir Kullolli is an International Student from Albania. He was attending Cerro Coso Community College in Ridgecrest, California when he was diagnosed with Aplastic Anemia. He was hospitalized on November 17, 1999. After getting better he transferred to Wentworth Institute of Technology in Boston, Massachusetts and graduated with a Bachelor of Science in Computer Engineering in December 2003. Now he's doing very well and he seems to be sick-free. Aplastic Anemia: An injury to the bone marrow; specifically the stem cells. Stem cells make red and white cells and platelets. The injury may be genetic, caused by viruses, drugs or other toxins. One known cause is an antibiotic used in Europe called Chloramphenocol. People who get this have a 1 in 30,000 chance of contracting blood disorders such as Aplastic Anemia. Ilir received this drug three years ago in Albania when he had appendicitis. The doctor is skeptical of this as a cause because of the time between it and the onset of the disease. [back to index] Blood elements Hemoglobin: Carries oxygen from the lungs to the body and Carbon Dioxide back to the lungs.
MedlinePlus Medical Encyclopedia: Idiopathic Aplastic Anemia
Anemia idiopathic aplastic. Definition Return to top. Idiopathic aplastic anemia is a failure of the bone marrow to properly form all types of blood cells
http://www.nlm.nih.gov/medlineplus/ency/article/000554.htm

Extractions: @import url(/medlineplus/images/advanced.css); Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: Bone marrow aspiration Antibodies Alternative names Return to top Anemia - idiopathic aplastic Definition Return to top Idiopathic aplastic anemia is a failure of the bone marrow to properly form all types of blood cells. Causes, incidence, and risk factors Return to top Idiopathic aplastic anemia is a condition that results from injury to the stem cell, a cell that gives rise to other cell types after it divides. Consequently, there is a reduction in all cell types red blood cells, white blood cells and platelets with this type of anemia , which is called pancytopenia. The cause of idiopathic aplastic anemia is unknown, but is thought to be an autoimmune process (the body reacting against its own cells). Causes of other types of aplastic anemia may be chemotherapy radiation therapy toxins , drugs, pregnancy, congenital disorder, or systemic lupus erythematosus Symptoms arise as the consequence of bone marrow failure. Low red blood cell count (anemia) leads to fatigue and weakness. Low white blood cell count (leukopenia) causes an increased risk of infection. Low platelet count (
MedlinePlus Medical Encyclopedia: Secondary Aplastic Anemia
Secondary aplastic anemia is a failure of the bone marrow to form enough blood cells. Secondary aplastic anemia results from injury to stem cells.
http://www.nlm.nih.gov/medlineplus/ency/article/000529.htm

Extractions: @import url(/medlineplus/images/advanced.css); Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: Bone marrow aspiration Blood types Alternative names Return to top Anemia - secondary aplastic; Acquired aplastic anemia Definition Return to top Secondary aplastic anemia is a failure of the bone marrow to form enough blood cells. All blood cell types are affected. Causes, incidence, and risk factors Return to top Secondary aplastic anemia results from injury to stem cells. Normal stem cells divide and differentiate into all blood cell types. Thus, when stem cells are injured, there is a reduction in red blood cells, white blood cells, and platelets. This condition can be caused by chemotherapy, drug therapy to suppress the immune system, radiation therapy, toxins such as benzene or arsenic, drugs, pregnancy, and congenital disorders. When the cause is unknown, it is then referred to as idiopathic aplastic anemia The disease may be acute or chronic and is usually gets worse unless the cause is removed.
MEdIC - Health Explorer - Iron Overload
MEdIC aplastic anemia patients who receive repeated blood cell transfussions may develop iron overload. A look at this condition and who needs treatment.
http://medic.med.uth.tmc.edu/ptnt/00001041.htm

Extractions: Iron Overload Aplastic anemia patients who receive repeated blood cell transfussions may develop iron overload. Iron from transfused red cells builds up in the blood and eventually accumulates in the heart, liver, pancreas, and endocrine organs. This excess iron may eventually damage vital organs and cause complications like liver disease, heart disease, and diabetes mellitus. Normal body iron stores are 3-4 grams. Each unit of transfused red cells contains 200-250 mg of iron. Thus, a patient who receives 2 units of blood each month would accumulate approximately 5-6 g of extra iron in one year. Without treatment to remove excess iron, damage to the heart and other organs occurs in patients who have received as few as 100 units of blood, or 20 grams of excess iron. Visible signs of iron overload, such as bronze or slate grey skin pigmentation, don't usually appear until enough iron has accumulated to cause tissue damage. In the United States, the only way to prevent or treat iron overload is with the iron chelating drug deferoxamine (Desferal). Desferal binds excess body iron and promotes its excretion by the kidneys in urine and via the bile in feces. Desferal is administered by subcutaneous or intravenous infusion by a small portable pump about the size of a Walkman. Typically the patient inserts a subcutaneous needle and wears the pump for 9-12 hours each day, usually at night while sleeping. Severely iron overloaded patients may need a continuous infusion through an indwelling central venous catheter. Several studies have demonstrated that regular chelation therapy with Desferal can remove excess body iron, prevent organ damage, and prolong life.
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins
aplastic anemia (AA) is the medical term for bone marrow failure. Though not a cancer, the treatment of aplastic anemia is often similar to therapies
http://www.hopkinskimmelcancercenter.org/cancertypes/aplastic-anemia.cfm?canceri
Fanconi Anaemia Resource Page
A rare disorder found in children that involves the blood and bone marrow. The symptoms include severe aplastic anemia, hypoplasia of the bone marrow, and patchy discoloration of the skin.
http://www.cancerindex.org/ccw/fanconi.htm

Extractions: Fanconi Anaemia Menu Cancer-Types Fanconi Anaemia Fanconi Anaemia is a rare disorder found in children that involves the blood and bone marrow. The symptoms include severe aplastic anemia , hypoplasia of the bone marrow, and patchy discoloration of the skin. This is an autosomal recessive condition, affected children usually develop severe aplastic anemia by age 8 to 9 years. Treatment usually consists of bone marrow transplant. Fanconi Anaemia is not a cancer, though recent research has shown an association between Fanconi Anaemia and leukaemia. There are 8 types of Fanconi Anaemia; known as complementation groups A through to H. Some definitions: Anemia below normal levels of erythrocytes (red blood cells) Aplastic anemia anemia that is resistant to treatment; often accompanied by deficiencies of other blood cells. Hypoplasia incomplete / under development of a part of the body. Pancytopenia deficiency of all types of blood cells. Recessive (genetics) if the required allele (a type of gene) is not present in both members of a pair of chromosomes then that allele is not expressed.
The Sidney Kimmel Comprehensive Cancer Center At Johns Hopkins
Since aplastic anemia is an autoimmune disorder resulting from the immune systems attack on blood stem cells, drugs that suppress the immune system do work
http://www.hopkinskimmelcancercenter.org/publications/publication.cfm?DocumentID
Aplastic Anemia
aplastic anemia patient resource center for patients, families, relatives and friends.
http://aplasticcentral.com/

Extractions: Cure for Low Platelet Counts. Aplastic Anemia is a rare disease requiring Bone Marrow Transplant which prevents Platelets and other blood cells from properly entering the blood stream. Platelets are counted and if they are low, a transfusion is required. There are only 300 new cases of Aplastic Anemia r eported each year. Aplastic Anemia is a function of low Platelets, and Bone Marrow Transplants are keywords that will help attract visitors to the site. Aplastic Anemia - Click Here to Enter Bone Marrow Transplant is the recommended cure for Aplastic Anemia with a matched sibling donor. If a Bone Marrow Transplant is not available from a sibling, then a Matched Unrelated Donor (MUD) may be used.
Aplastic Anemia / Family Village Library
The aplastic anemia Foundation of America provides free educational materials and A listserve based mailing list in support of aplastic anemia (AA) and
http://www.familyvillage.wisc.edu/lib_apls.htm

Extractions: http://www.aplastic.org/ The Aplastic Anemia Foundation of America provides free educational materials and updated medical information, serves as a resource directory for patient assistance and emotional support, and financially support research for Aplastic Anemia and related syndromes. AAFA publishes a quarterly newsletter at no charge. There are also various publications and fact sheets available including, Drug Therapy, and Bone Marrow Transplantation. They have audio tapes and books that are free, and are printed in English, Spanish, French, and Japanese. Aplastic Anemia
Aplastic Anemia: Pathophysiology And Treatment
Likewise, the therapy of aplastic anemia has evolved as studies of both bone Fanconi s anemia. Part I, Pathophysiology of acquired aplastic anemia
http://www.bloodline.net/stories/storyReader$1702

Extractions: Cambridge University Press, n.p., 2000, 391 pages, hardbound. Significant progress has been made in the past several years in understanding the pathophysiology and causes of aplastic anemia. Likewise, the therapy of aplastic anemia has evolved as studies of both bone marrow transplantation and immunosuppressant treatments have been performed and have matured. This book is an effort to provide a concise and up-to-date summary of the currently established body of information on the pathophysiology and treatment of aplastic anemia. The editors indicate that the genesis of the book lay within the aplastic anemia working party of the European Group for Blood and Marrow Transplantation (EBMT). This book is intended for those who desire a deeper understanding of the pathophysiology of aplastic anemia and for those needing practical information on the management of patients with this disorder. A special chapter is devoted to children with acquired aplastic anemia and there is also a chapter on clonal transformation. This section ends with a chapter entitled, "Guidelines for treating aplastic anemia" which is, in fact, a concensus document from a group of international experts. Overall, this section is quite good with a thorough review of bone marrow transplantation and immunosuppressive therapy. The guideline section is practical and well written. Disappointingly, there is little review of an intriguing recent therapy for aplastic anemia using high-dose cyclophosphamide without stem cell infusion. Moreover, although this text is reasonably up-to-date in most sections, some areas are already becoming anachronistic, such as, the advice that allogeneic peripheral blood stem cells are experimental and should not be used.
Allogeneic Marrow Grafts For Aplastic Anemia
Allogeneic Marrow Grafts for aplastic anemia Patients With aplastic anemia for Allogeneic Marrow Transplantations The Experience in Four Centers
http://www.bloodline.net/stories/storyReader$2533

Extractions: Login Cyclophosphamide and Antithymocyte Globulin to Condition Patients With Aplastic Anemia for Allogeneic Marrow Transplantations: The Experience in Four Centers Rainer Storb, Karl G.Blume, Margaret R.O'Donnell, Tom Chauncey, Stephen J.Forman, H.Joachim Deeg, Wendy W.Hu, Frederick R.Appelbaum, Kris Doney, Mary E.D.Flowers, Jean Sanders, Wendy Leisenring Biology of Blood and Marrow Transplantation 7:39-44 (2001)
Aplastic Anemia - Lucile Packard Children's Hospital
aplastic anemia occurs when the bone marrow produces too few of all types of blood Nearly 50 to 75 percent of childhood cases of aplastic anemia occur
http://www.lpch.org/DiseaseHealthInfo/HealthLibrary/hematology/aplsanem.html

Extractions: Effects of Pediatric Brain Tumors and Their Treatment Haunt Survivors for Years, Stanford/Packard Study Finds Aplastic Anemia Aplastic anemia occurs when the bone marrow produces too few of all types of blood cells: red cells, white cells, and platelets. A reduced number of red blood cells causes the hemoglobin (a type of protein in the red blood cells that carries oxygen to the tissues of the body) to drop. A reduced number of white blood cells causes the patient to be susceptible to infection. A reduced number of platelets can cause the blood not to clot as easily. Aplastic anemia in children has multiple causes. Some of these causes are idiopathic, meaning they occur sporadically for no known reason. Other causes are secondary, resulting from a previous illness or disorder.
Aplastic Anemia
aplastic anemia information and links add your link!
http://www.doctorpage.com/findit/Diseases_and_Conditions/Aplastic_Anemia/

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