Hereditary hemochromatosis

From WikiMD.org
Jump to navigation Jump to search
Hereditary hemochromatosis
TermHereditary hemochromatosis
Short definitionhereditary hemochromatosis (heh-REH-dih-tayr-ee HEE-moh-kroh-muh-TOH-sis) An inherited condition that causes excess iron buildup in the body. The excess iron is stored in the body's tissues and organs, particularly the liver, heart, pancreas, skin and joints. 
TypeCancer terms
SpecialtyOncology
LanguageEnglish
SourceNCI
Comments


hereditary hemochromatosis - (pronounced) (heh-REH-dih-tayr-ee HEE-moh-kroh-muh-TOH-sis) An inherited condition that causes excess iron buildup in the body. The excess iron is stored in the body's tissues and organs, particularly the liver, heart, pancreas, skin and joints. This can lead to liver disease, heart problems, diabetes and organ failure. Symptoms include skin color changes, joint and abdominal pain, fatigue, and loss of sex drive. Patients with hereditary hemochromatosis also have an increased risk of liver cancer. There are five types of hereditary hemochromatosis. Each type is caused by changes in different genes. Symptoms for each type typically begin at different ages. Type 1 hemochromatosis is one of the most common genetic disorders in the United States

External links

Esculaap.svg

This WikiMD article is a stub. You can help make it a full article.


Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski