What does HH mean in MEDICAL
Hereditary Haemochromatosis (HH) is a genetic disorder that causes the body to absorb too much iron from food. This can lead to a build-up of iron in the body's organs, which can damage them and cause serious health problems. HH is a common genetic disorder, affecting around 1 in 200 people in the UK. It is more common in men than in women.
HH meaning in Medical in Medical
HH mostly used in an acronym Medical in Category Medical that means Hereditary Haemochromatosis
Shorthand: HH,
Full Form: Hereditary Haemochromatosis
For more information of "Hereditary Haemochromatosis", see the section below.
What is HH?
HH is a genetic disorder that affects the way the body absorbs iron from food. In people with HH, the body absorbs too much iron, which can lead to a build-up of iron in the body's organs. This can damage the organs and cause serious health problems.
Symptoms of HH
The symptoms of HH can vary depending on the severity of the condition. In the early stages, people with HH may not have any symptoms. As the condition progresses, symptoms can include:
- Fatigue
- Weakness
- Joint pain
- Abdominal pain
- Liver damage
- Heart failure
- Diabetes
Diagnosis of HH
HH is diagnosed with a blood test that measures the amount of iron in the blood. A liver biopsy may also be necessary to confirm the diagnosis.
Treatment of HH
The treatment for HH is to remove excess iron from the body. This can be done with bloodletting, which is a procedure that removes blood from the body. Iron chelation therapy can also be used to remove excess iron from the body.
Essential Questions and Answers on Hereditary Haemochromatosis in "MEDICAL»MEDICAL"
What is Hereditary Haemochromatosis (HH)?
Hereditary Haemochromatosis (HH) is an inherited genetic disorder that causes the body to absorb too much iron from food. This excess iron is stored in organs and tissues, leading to tissue damage and organ failure.
What causes HH?
HH is caused by mutations in genes involved in iron regulation. These mutations lead to impaired iron absorption and iron overload in the body.
What are the symptoms of HH?
Symptoms of HH can vary, depending on the severity of iron overload. Early symptoms may include fatigue, weakness, joint pain, and abdominal pain. As iron overload progresses, more severe symptoms can develop, such as liver damage, heart failure, diabetes, and skin discoloration.
How is HH diagnosed?
HH can be diagnosed through blood tests that measure iron levels, genetic testing to identify mutations, and liver biopsy to assess liver damage.
How is HH treated?
Treatment for HH involves removing excess iron from the body. This can be done through regular blood transfusions, which remove iron-rich red blood cells. Iron chelators, which are medications that bind to iron and promote its excretion, may also be used.
Can HH be prevented?
HH cannot be prevented, as it is an inherited condition. However, early diagnosis and treatment can help prevent or delay complications.
What is the outlook for people with HH?
With proper treatment, people with HH can live long and healthy lives. However, untreated HH can lead to serious complications and reduced life expectancy.
Final Words: HH is a serious genetic disorder that can lead to a build-up of iron in the body's organs. This can damage the organs and cause serious health problems. However, HH can be treated with bloodletting or iron chelation therapy.
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