2025年1月9日 · Hemochromatosis (he-moe-kroe-muh-TOE-sis) is a condition that causes the body to absorb too much iron from food. Excess iron is stored in the organs, especially the liver, heart and pancreas. Too much iron can lead to life-threatening conditions, such as liver disease, heart problems and diabetes.

2025年1月9日 · Treating hemochromatosis can help relieve symptoms of tiredness, stomach pain and skin darkening. It can help prevent serious complications such as liver disease, heart disease and diabetes. If you already have one of these conditions, phlebotomy may …

2025年1月9日 · Un gen que se llama HFE es la causa más frecuente de la hemocromatosis hereditaria. Heredas un gen HFE de cada uno de tus padres. El gen HFE tiene dos mutaciones comunes, C282Y y H63D.

2025年1月9日 · hfe 基因是导致遗传性血色素沉着症的主要原因。您可能会从父母各方分别遗传一个 hfe 基因。hfe 基因有两种常见的突变：c282y 和 h63d。基因检测可确定 hfe 基因是否存在这些变化。 如果遗传了两种变化基因，则可能会患上血色素沉着症。您也可能将变化的基因传 ...

2024年11月7日 · The Hereditary Hemochromatosis Clinic located on Mayo Clinic's campus in Florida provides state-of-the-art diagnostics, treatments and education to patients who have hereditary hemochromatosis or who are at risk of developing it.

2025年1月9日 · Se recomienda analizar el ADN para detectar cambios en el gen HFE si tienes altos niveles de hierro en la sangre. Si estás considerando la posibilidad de realizarte pruebas genéticas para detectar la hemocromatosis, habla de las ventajas y desventajas con el proveedor de atención médica o un consejero genético.

While I know JAK2, TET2, CALR, etc. are the most common genetic mutations in PV, does anyone else have it with the HFE gene (with or without hereditary hemochromatosis) and/or IFT140 (with or without polycystic kidney disease?

غالبًا يكون سبب الإصابة بداء ترسب الأصبغة الدموية الوراثي جين يُسمى hfe. فأنت ترث جين HFE واحدًا من كلا والديك. ويحتوي جين HFE على طفرتين شائعتين؛ هما C282Y و H63D.

2025年1月9日 · 如果血液中含有高水平的铁，建议您检测 dna 中的 hfe 基因是否突变。如果您正在考虑对血色素沉着症进行基因检测，请向医务人员或遗传咨询师咨询这方面的利弊。 取肝组织样本进行检测。如果医务人员怀疑存在肝脏损伤，可能会安排进行肝脏活检。

2016年12月16日 · Treatment for hereditary hemochromatosis involves removing a pint of blood from the body on a weekly basis, a process called therapeutic phlebotomy. The goal is to reduce iron levels to normal. Dr. Palmer recommended that Chad have a catheter port placed to make weekly blood draws less painful.