61. Porphyrias: Clinical Manifestations, Diagnosis And Treatment MEDSTUDENTS-METABOL A short review of hemochromatosis, giving atention mainly to its etiology, clinical manifestations, treatment and prognosis.Importance about early diagnosis is http://www.medstudents.com.br/metdis/metdis4.htm

METABOLIC DISORDERS Medstudents' Homepage Hemochromatosis Definition Hemochromatosis is a disease due to increased iron absorption that leads to accumulation of iron in diverse tissues. Classification It can be hereditary (primary hemochromatosis) or secondary to chronic anemias as ß-thalassemias (ineffective erythropoiesis leading to increased erythrocitic destruction) or defects in hemoglobin synthesis ( as in porphyria cutanea tarda) ;multiple transfusion therapy ;or others less common conditions. Pathogenesis Iron absorption from the gut occurs normally in a rate of 1 mg per day. In hemochromatosis this absortion reaches the rate of 4 to 5 mg/d and there is a progressive accumulation to 15 to 40 grams of body iron (normal ~ 2 to 3 g). Thus, the disease develops in men above age 20 and postmenopausal women, due to stopping in iron loss in menses. The iron accumulates in every tissue of the body, but main clinical manifestations are secondary to iron deposition in: Liver, thyroid, hypothalamus, heart, pancreas, gonads and joints. Clinical Manifestations Many patients are asymptomatic. Common symptoms are fatigue, arthalgias, impotence, amenorrhea and palpitations. The most characteristical clinical manifestation occur in the liver because the portal circulation filters the iron initially absorbed fom the gut. Usually patients develop cirrhosis. Heart manifestations include arrythmias and disturbances of conduction. Skin adquires an diffuse hyperpigmentation mainly in scars, sun exposed and unexposed areas and genitalia. Arthropathy occurs in wrists, hips, knees and ankles. To distinguish this arthopathy from others, searching for initial involvement of second and third metacarpophalangeal joints is helpful. Hypogonadism hipogonadothrofic is secondary to iron deposition in hypophisary cells and leads to loss of libido, amenorrhea, impotence and body hair losing. Diabetes Mellitus results from pancreatic accomitment and the signs and symptons, as the treatment, do not differ from conventional diabetes.

62. Recognition And Management Of Hereditary Hemochromatosis - March 1, 2002 - Ameri American Family Physician. Recognition and Management of Hereditary hemochromatosis. Hereditary hemochromatosis is associated with mutations in the HFE gene. http://www.aafp.org/afp/20020301/853.html

Advanced Search Recognition and Management of Hereditary Hemochromatosis DAVID J. BRANDHAGEN, M.D., VIRGIL F. FAIRBANKS, M.D., and WILLIAM BALDUS, M.D. Mayo Medical School, Rochester, Minnesota Hereditary hemochromatosis is the most common inherited single-gene disorder in people of northern European descent. It is characterized by increased intestinal absorption of iron, with deposition of the iron in multiple organs. Previously, the classic description was combined diabetes mellitus, cutaneous hyperpigmentation and cirrhosis. Increasingly, however, hereditary hemochromatosis is being diagnosed at an earlier, less symptomatic stage. The diagnosis is based on a combination of clinical, laboratory and pathologic findings, including elevated serum transferrin saturation. Life expectancy is usually normal if phlebotomy is initiated before the development of cirrhosis or diabetes mellitus. Hereditary hemochromatosis is associated with mutations in the HFE gene. Between 60 and 93 percent of patients with the disorder are homozygous for a mutation designated C282Y. The

63. Hemochromatosis hemochromatosis The Liver The liver is the largest organ in the body. What is hemochromatosis? hemochromatosis is commonly known as iron overload disease. http://www.gicare.com/pated/ecdlv36.htm

Home Jackson Gastro Patient Education Hemochromatosis The Liver The liver is the largest organ in the body. It is found high in the right upper abdomen, behind the ribs. It is a very complex organ and has many functions. They include: Storing energy in the form of sugar (glucose) Storing vitamins, iron, and other minerals Making proteins, including blood clotting factors, to keep the body healthy and help it grow Processing worn out red blood cells Making bile which is needed for food digestion Metabolizing or breaking down many medications and alcohol Killing germs that enter the body through the intestine The liver shoulders a heavy work load for the body, and almost never complains. It even has a remarkable power to regenerate itself. Still, it should not be taken for granted. The liver is subject to illnesses that can lead to permanent damage. One example is autoimmune hepatitis, a condition in which the body fights against its own liver. What is Hemochromatosis? Hemochromatosis is commonly known as iron overload disease. A malfunction in the way iron is absorbed from the intestinal tract causes the body to absorb and store too much iron. Certain vitamins and minerals are normally stored in the liver, and iron is one of them. However, too much iron stored in the liver can damage it. With hemochromatosis, excess iron is also deposited in other organs and tissues, especially the heart and pancreas, causing damage to these organs, too. This disease occurs more commonly than was originally thought. It is estimated that hemochromatosis affects about one in every 300-400 people. Occasionally, a secondary type of iron overload (called hemosiderosis) occurs in people who take large amounts of iron supplements, or in people who must have repeated blood transfusions, or who have certain other diseases. However, the body usually returns to normal processing of iron when the excess intake is eliminated.

64. Diabetes Types, Hemocromatosis hemochromatosis Can Cause Diabetes. hemochromatosis is an inherited disease that causes excessive amounts of iron to accumulate in the body. http://www.diabetesnet.com/diabetes_types/hemocromatosis.php

Forums Contest Site Map Info Store Related Products Using Insulin Newsletter Get diabetes information by email! Archives Forum Visit our Diabetes Forums to discuss your concerns about diabetes. Types of Diabetes People Insulins What Type You Have Type 1 ... Gestational Diabetes Hemocromatosis Cystic Fibrosis Hemochromatosis Can Cause Diabetes by John Walsh, P.A., C.D.E. Hemochromatosis is an inherited disease that causes excessive amounts of iron to accumulate in the body. Although diabetes can be one of many unwanted side effects of the iron overload, the rate of hemochromatosis is no higher in those with diabetes than those without. Diabetes caused by damage to the pancreas occurs after many years of hemochromatosis. In one French study, diabetes was found in 40% of 115 people at the time their hemochromatosis was diagnosed (Acta Clin Belg 1999 Dec; 54(6): pgs. 334-45). This type of secondary diabetes is often referred to as "bronze diabetes" because it is sometimes accompanied by a bronze color of the skin. Screening for hemochromatosis should be done in people with diabetes who also have liver disease. Hemochromatosis is the most common genetic disease in this country with 13% of the population carrying the gene, and one in every 200 people having it.

65. Kimball Genetics - Hemochromatosis DNA Test A laboratory specializing in genetic testing and counseling for hemochromatosis, venous thrombosis, fragile X and other common disorders. http://www.kimballgenetics.com/tests-hemochrom.html

Hemochromatosis DNA Test Hereditary Hemochromatosis (HH) is the most common genetic disorder known, with a prevalence of 1/200 and a carrier frequency of 1/8 in Caucasians. This disorder involves excess iron absorption and storage in organs and leads to high morbidity and mortality if untreated. Historically, most cases have remained undiagnosed until late in the course of the disease when irreversible damage has already occurred. Early diagnosis allows for prevention of symptoms through treatment by phlebotomy. Two mutations associated with hemochromatosis have been discovered in the HFE gene. The major mutation, Cys282Tyr (also known as 845A) is present in the homozygous state in 85% of Caucasians with clinically diagnosed hemochromatosis. Most homozygotes (with two copies of the mutation) and some heterozygotes (with one copy of the mutation) develop iron overload and hemochromatosis. A second mutation, His63Asp (also known as 187G), appears to somewhat increase risk of iron overload. Although only a small percent of individuals (up to 6%) with this mutation develop hemochromatosis, DNA testing for hemochromatosis provides for effective early diagnosis and prevention. Indications for Hemochromatosis DNA Testing: Clinical diagnosis of hemochromatosis Unexplained elevated serum concentrations of liver enzymes Cirrhosis, liver failure, or hepatocellular carcinoma

66. CLF : Hemochromatosis hemochromatosis What is hemochromatosis? hemochromatosis is an inherited disease in which the body absorbs too much iron from the diet. http://www.liver.ca/english/liverdisease/hemochromatosis.html

CLF Regional Offices Find a Location BC/Yukon Alberta Saskatchewan Manitoba GTA S.W. Ontario Central Ontario S.E. Ontario Quebec Atlantic Can. HEMOCHROMATOSIS What is Hemochromatosis? Hemochromatosis is an inherited disease in which the body absorbs too much iron from the diet. Hemochromatosis is one of the most common genetic diseases in Canada affecting 1 in 327 Canadians. Normally, only enough iron to meet the body's daily requirements is absorbed; the remainder is usually excreted through the bowels. In hemochromatosis, however, iron continues to be absorbed and stored in different organs and tissues long after body needs are met. The liver is the first organ to store iron and when its storage capacity is exhausted, the iron continues to accumulate in the heart, the pituitary gland and elsewhere in the body. If untreated, damage to the liver, heart, and pancreas may eventually lead to death. What causes hemochromatosis? Hemochromatosis is hereditary. In order to have the disease, a patient must have inherited two defective genes, one from each parent; siblings of an affected individual have a 25 per cent chance of getting this disease. Children are less likely to be affected since the other parent must be a carrier of a hemochromatosis gene. What are the symptoms of hemochromatosis?

67. Iron_enemy S Home Page God Bless. There is a support group of people who have hemochromatosis, or someone in their family has it. hemochromatosis. Are You Dying From Too Much Iron? http://www.geocities.com/HotSprings/Villa/6540/

I AM VERY HONORED TO HAVE RECEIVED THESE AWARDS Please click on the awards and learn about who gives them and others who have received them. You will read some heart warming stories. WE ALL HAVE CROSSES TO BEAR Thank you for visiting my site. I worked very hard to get it just right, plus this is my first site. The main reason was to get you to read it, for the information may save your life. Please allow time to load, read it, enjoy the graphics, and sign my guestbook on your way out. God Bless. There is a support group of people who have Hemochromatosis, or someone in their family has it. Join the group for support and information. Click below to subscribe to FHHF. Click to subscribe to FHHF YOU ARE VISITOR HEMOCHROMATOSIS Are You Dying From Too Much Iron? Never heard of this disease, HEMOCHROMATOSIS? Neither had I until I was diagnosed with it. It's not a pretty disease if not caught in time. As a matter of fact, it's a KILLER. It's assumed now that my father died, at the age of 68, from it, but the death certificate

68. National Human Genome Research Institute - Learning About Hereditary Hemochromat Answers to frequently asked questions about hereditary hemochromatosis, published by the National Human Genome Research Institute. http://www.genome.gov/10001214

Talking Glossary of Genetic Terms Frequently Asked Questions about Genetics Clinical Research Online Health Resources ... Specific Genetic Disorders Learning About Hereditary Hemochromatosis Learning About Hereditary Hemochromatosis What do we know about hereditary hemochromatosis? Is there a test for hereditary hemochromatosis? NHGRI Clinical Research on Hereditary Hemochromatosis Additional Resources for Hereditary Hemochromatosis Information What do we know about hereditary hemochromatosis? Hereditary hemochromatosis (HH) is a genetic disease that alters the body's ability to regulate iron absorption. If correctly diagnosed, HH is easily and effectively treated, but if untreated, it can lead to severe organ damage. Caucasians of northern European descent are at highest risk. An estimated one million people in the United States have hereditary hemochromatosis. HH causes the body to absorb too much iron. Normally humans extract needed iron from food via the intestines. When there is an adequate amount of iron, the body reduces its absorption to avoid excessive accumulations. In a person with HH, the mechanism for regulating iron absorption is faulty and the body absorbs too much iron. Over time - several years - this excess iron is deposited in the cells of the liver, heart, pancreas, joints and pituitary gland, leading to diseases such as cirrhosis of the liver, liver cancer, diabetes, heart disease and joint disease.

69. Hemochromatosis.be Webpage still under construction. Soon you will see information here about hemochromatosis. Please visit us again soon. For info mail info@hemochromatosis.be. http://www.hemochromatosis.be/

Webpage still under construction. Soon you will see information here about Hemochromatosis. Please visit us again soon. For info mail info@hemochromatosis.be Website in aanmaak. Binnenkort vind u hier meer informatie over Hemochromatose. Kom geregeld langs om updates te zien. Voor info mail info@hemochromatosis.be Site en construction. Des informations sur Hemochromatos seront bientôt disponible ici. Visitez ce site régulièrement. Pour info, envoyez-nous un email info@hemochromatosis.be

70. Hemochromatosis: Iron Storage Disease hemochromatosis (Iron Storage Disease). Yet with this massive overdosing of iron, none of the birds had developed hemochromatosis. http://www.starlingtalk.com/hemochromatosis.htm

Care and Rehabilitation of Injured and Orphaned Starlings Home Baby Starlings Adult Diet Pet Starlings ... Message Board Hemochromatosis (Iron Storage Disease) Iron storage is not usually caused by dietary iron, but some years ago the theory was that perhaps the iron in the diets of some captive birds was causing the overload of iron, and some genetic factor was the reason for it. Hemochromatosis is not known to be in wild populations of birds; it is considered to be a disease of captive birds, yet in the wild, a mynah's main diet is figs, which have a very high iron content; if this were a genetic problem, then you would expect to see it in wild populations. Green Tea. Additionally, Zhi Zhong, PhD, from the University of North Carolina at Chapel Hill, and colleagues looked at whether the powerful, free-radical scavenging antioxidants in green tea could alleviate some of the problems associated with fatty livers. They found that "Green tea extract scavenges harmful free radicals in fatty livers and therefore could be an effective treatment to prevent failure of liver transplants." In a study at Brookfield Zoo, fifty eight European Starlings were studied after feeding one group a low iron diet of 148 ppm and the other group a high iron diet of 3,035 ppm of iron. All birds were euthanized after four months and tested for iron storage. Birds in both groups had similar liver iron content, but the birds on the high iron diet had significantly higher values. Yet with this massive overdosing of iron, none of the birds had developed Hemochromatosis.

71. Hemochromatosis A chapter from The Cleveland Clinic Disease Management Project written by Anthony S. Tavill, MD, which discusses hemochromatosis. The Cleveland Clinic. http://www.clevelandclinicmeded.com/diseasemanagement/gastro/hemochromatosis/hem

Published August 13, 2002 Anthony S. Tavill, MD Department of Gastroenterology and Hepatology Print Chapter The Cleveland Clinic Foundation There are many inherited metabolic diseases that may have a pathologic impact on the liver. In many cases the liver component of these diseases is only an epiphenomenon of a more generalized systemic disorder. Examples of such epiphenomena are glycogen and lipid storage diseases in which hepatomegaly is a manifestation of the underlying metabolic defect although the liver is not necessarily the major target organ. However, there are three genetically determined diseases in which the liver may be the principal target organ, with manifestations of acute, subacute, or chronic disease that may become evident in early or later life. These are hereditary hemochromatosis (HH), a major disorder of iron overload; Wilson's disease , a genetic disorder of copper overload; and

72. Hemochromatosis hemochromatosis information and links to national and international support groups, clinics with genetic counselors and geneticists. hemochromatosis. http://www.kumc.edu/gec/support/hemochro.html

Hemochromatosis Iron overload American Hemochromatosis Society, Inc. (AHS) 777 East Atlantic Avenue, Z-363, Delray Beach, Florida U.S.A. 33483-5352 Email: ahs@emi.net Web site: www.americanhs.org Iron Overload Diseases Association, Inc. (IOD) 433 Westwind Drive, N. Palm Beach, FL 33408 Phone: 561.840.8512 - Fax: 561.842.9881 Website: www.ironoverload.org E-mail : iod@ironoverload.org Canadian Hemochromatosis Society 272-7000 Minoru Blvd., Richmond, BC, Canada V6Y 3Z5 Phone: 877.223.4766, toll-free in Canada only, or 604.279.7135 Fax. 604.279.7138 E-mail: office@cdnhemochromatosis.ca Hemochromatosis Foundation, Inc. PO Box 8569, Albany, NY 12208 Phone: 518.489.0972 - Fax: 518.489.0227 Web site: www.hemochromatosis.org Haemochromatosis Society Australia, Inc. 412 Musgrave Road, Coopers Plains, Australia Phone: 07 3345 7583 - Fax: 07 3345 8051 E-mail: margaret@haemochromatosis.org Web site: www.haemochromatosis.org/ Haemochromatosis Society , England Association Hemochromatose , France Hemochromatosis , Belgium Also See: National organizations , information on genetic conditions or birth defects Hemochromatosis Pamphlet , American Liver Foundation Hemochromatosis , Iron Disorders Institute National Digestive Diseases Information Clearinghouse (NDDIC) , National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health Hemochromatosis case study CDC webcast, May 2000, public health and genetics, view online

73. Hemochromatosis, Inflammation And Anemia hemochromatosis, inflammation and anemia. The HFE gene is mutated in patients suffering from the common iron overload disease hemochromatosis. http://www.eurekalert.org/pub_releases/2004-04/embl-hia041504.php

Public release date: 18-Apr-2004 Contact: Trista Dawson dawson@embl.de European Molecular Biology Laboratory Hemochromatosis, inflammation and anemia Researchers discover a surprising link Patients with inflammatory diseases such as arthritis, chronic infections and some types of cancer, often become anemic – a condition called anemia of chronic disease (ACD). While ACD rarely kills patients, it can make their lives miserable. A discovery at EMBL, in collaboration with researchers at Children's Hospital Boston and Harvard Medical School, now links the gene HFE to ACD. The HFE gene is mutated in patients suffering from the common iron overload disease hemochromatosis. This finding gives hope that one day an effective and specific therapy may be developed to treat ACD (featured in Nature Genetics , April 18, 2004). When people are infected with microbes, the level of iron in their blood drops. This has an important function: iron is essential for the growth of infectious microbes, so one way for the body to fight back is to lower the amount of iron in circulation. "Unfortunately, while this decrease in iron hinders the spread of parasites and is beneficial in the short term, it can cause anemia," notes EMBL Group Leader Matthias Hentze. "During a long term inflammatory condition, low levels of iron can starve the bone marrow of this metal which is essential for blood cells, leading to ACD."

74. Hemochromatosis Informs patients about hemochromatosis, an inborn error of iron metabolism, which can lead to liver cirrhosis, liver cancer and heart failure. http://www.ikp.unibe.ch/lab2/hemce.html

HEMOCHROMATOSIS Prof. Dr. med. J. Reichen Dept. of Clinical Pharmacology, University of Berne Deutsch, bitte 1. Prevalence and cause: Hemochromatosis is the most prevalent genetic disease of adults. One in 10 carries the faulty gene and 1/400 will get the disease. Based on this gene frequency we have to assume that in the Swiss population there are 17'500 - 20'000 patients affected. The main mutation in the gene, now called HFE, was described in 1996 by Feder and colleagues. The mutation leads to uncontrolled absorption of iron and deposition of this potentially toxic heavy metal in different organs. 2. What are the signs and symptoms? The first symptoms can originate from the liver, the articulations, the pancreas, the heart and endocrine glands. This first signs can be very subtle and the diagnosis is missed if the treating physician does not think about the possibility of hemochromatosis. Liver Fatigue, dull aches or pains in the upper belly Articulations Inflammation, pain and swelling Pancreas Diabetes (thirst, increased urination)

75. Dr. Rose's Peripheral Brain--HEMOCHROMATOSIS hemochromatosis. I. Pathophysiology. Often get macrocytosis ( due to liver dysfunction ?); Genetic screens (for hereditary hemochromatosis). http://faculty.washington.edu/momus/PB/hemochro.htm

HEMOCHROMATOSIS I. Pathophysiology Iron overload causing tissue damage Can be hereditary (mostly Caucasian), in which case excess intestinal absorption of iron occurs In the hereditary form, clinical manifestations occur after years of excess absorption Women homozygous for the hereditary defect express the disease 1/10 as often as men, prob. b/c of menstrual loss of iron Ethanol abuse or hepatitis accelerates liver and pancreatic damage, prob. due to high serum levels of ferritin after hepatocyte injury A candidate gene has been identified: HFEsee below Or secondary, caused by Chronic anemias, e.g. homozygous beta-thal Multiple transfusions Porphyria cutanea tarda Portocaval shunt, etc. Iron accumulation-ubiquitous, as ferritin and hemosiderin Liver All Fe absorbed from intestine passes through liver; any Fe that exceeds binding capacity of transferrin is deposited Pancreas, heart, gonads, thyroid, hypothalamus, pituitary, and joints, causing dysfunction in all these organs

76. HEMOCHROMATOSIS IN LORIES hemochromatosis IN LORIES. Margrethe Warden. hemochromatosis atra). In most cases, hemochromatosis is asymptomatic until shortly before death. http://www.lorikeets.com/hemochromatosis.htm

HEMOCHROMATOSIS IN LORIES Margrethe Warden There have not been many studies conducted on avian hemochromatosis; therefore, much of what is commonly believed about the disorder is speculation. Most of the information relating to Iron Storage Disease and lories is anecdotal and as such is not always appropriate data for an actual scientific discussion. I began learning more about this condition in 1999 when it was discovered in sev eral of my own lories, specifically in five of my black lories ( Chalcopsitta atra). This disorder usually shows up in lories around five or six years of age; however, it has been discovered in much younger birds than that who have been fed a diet high in iron content. It is ultimately a fatal disorder that can take months, even years, to develop and become severe enough to result in death. The prevalence of hemochromatosis in lories is not well documented; therefore, it is not known if it has become a common problem in our captive population. The lack of documentation underscores the importance of performing a complete necropsy on every lory that dies. A liver stain can diagnose iron storage. Even when hemochromatosis does not appear to be the primary cause of death, it is important to conduct the histopathology to determine if the disorder was developing in the individual. Only through these tests and the compilation of information will the pervasiveness of this disease be documented and understood. Since most lory species are no longer being imported into this country, we must be diligent in maintaining the good health of the existing population.

77. Hereditary Hemochromatosis Your 68year-old Irish uncle was just diagnosed with hereditary hemochromatosis, a genetic disorder common among people of Northern European descent. http://kidshealth.org/parent/general/aches/hh.html

KidsHealth Parents General Health Your 68-year-old Irish uncle has diabetes and has also been bothered lately by chronic fatigue and a swollen stomach. After seeing his doctor, he still isn't feeling well. Finally, he visits a new doctor who diagnoses him with hereditary hemochromatosis, a genetic disorder common among people of Northern European descent. You've never heard of this condition before, and now your head is spinning with questions. Could other family members have it? What are the symptoms? Are you at risk? Should you be concerned for your children? It's time to learn more! What Is Hereditary Hemochromatosis? A genetic disease that causes the body to absorb and store too much iron , the condition gets its name from "hemo" for blood and "chroma" for color, referring to the characteristic bronze skin tone that iron overload can cause. Someone with hereditary hemochromatosis who has never taken an iron supplement could find out in later years that iron overload is causing serious health problems. Iron is a trace mineral that plays a vital role in the body. Every red blood cell contains iron in its hemoglobin, the pigment that carries oxygen from the lungs to the tissues. We get iron from our diet, and normally the body absorbs approximately 10% of the iron found in foods. People with hemochromatosis absorb double that amount.

78. Hemochromatosis Home Browse Resources What s Next Help Comments?. hemochromatosis. Also spelled HAEMOCHROMATOSIS, also called IRON STORAGE http://www.cs.odu.edu/~wild/DiabetesWeb/education/hemochromatosis.html

Home Browse Resources What's Next ... Comments? Hemochromatosis Also spelled HAEMOCHROMATOSIS, also called IRON STORAGE DISEASE, or BRONZE, inborn metabolic defect characterized by an increased absorption of iron, which accumulates in body tissues. The clinical manifestations include skin pigmentation, diabetes, enlargement of the spleen and liver, heart failure, and general weakness and lassitude. In males, the symptoms are usually noted after 35 years of age, and in females, after menopause, when iron is no longer lost through menstruation and pregnancy. Treatment consists of the removal of blood at regular intervals to decrease the concentration of body iron.

79. Hemochromatosis - Information / Diagnosis / Treatment / Prevention home genetic disorders hemochromatosis hemochromatosis. Iron Overload Diseases Association Information on hemochromatosis. http://www.healthcyclopedia.com/genetic-disorders/hemochromatosis.html

Home Health cyclopedia All Topics by Category The Good Health Search Engine Health Conditions A-Z Gurus ... genetic disorders > hemochromatosis Hemochromatosis Information / Diagnosis / Treatment / Prevention External links (marked with an arrow ) open in a new window. This site is a web directory and does not offer medical advice. We cannot take responsibility for information found on listed sites. This Page Related Topics Medical Definition Health Portals Health News ... Web Directory: Related Topics: Medicine/Medical Specialties/Hematology Nutrition and Metabolism Disorders Medical Definition: University of Newcastle-upon-Tyne Medical Dictionary: "haemochromatosis" Health Portals: Johns Hopkins Medicine MayoClinic.com Health News: Search millions of published articles for news on Hemochromatosis Modern Medicine Aging The Ardell Wellness Report HealthFacts Medical Post Medical Update Men's Health and the National Women's Health Report Note: Subscription required to access the full text of articles. Web Directory: American Hemochromatosis Society This organisation provides information and educates the public about hemochromatosis. They publish a newsletter and have an online support group. Canadian Hemochromatosis Society Information about the symptoms, diagnosis and treatment of hemochromatosis.

80. Hemochromatosis Information What is hemochromatosis? Usually, excess iron that the body doesn t need is excreted. But in hemochromatosis, the excess iron is stored in the body. http://www.mamashealth.com/hemo.asp

Mamashealth.com Home Digestive Health Pages Appendicitis Celiac Disease Children With Ulcers Cholecystitis ... Zollinger-Ellison Links What is Hemochromatosis? Hemochromatosis, (he-mo-kro-ma-toe-sis) also called hereditary hemochromatosis or HHC is a hereditary disorder in which the body absorbs too much iron from food. Usually, excess iron that the body doesn't need is excreted. But in hemochromatosis, the excess iron is stored in the body. Some of the places it is stored are: the pancreas, liver, and skin. The excess iron damages these organs and tissues. What are the Symptoms? Some of the most common symptoms of hemochromatosis are: fatigue, abdominal pain, jaundice (yellowing of skin and eyes), and a change in skin color to bronze or gray. Long Term Affects? Over time, hemochromatosis can cause liver disease, liver failure, liver cancer heart disease diabetes , impotence for men, and infertility and loss of periods for women. How is Hemochromatosis diagnosed? Hemochromatosis is diagnosed through blood tests that measure iron levels. If your doctor thinks liver damage has occured, a liver biopsy can be done to check for the amount of iron in the liver and for liver damage. How is it Treated?

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