n.血色病，血色素沉着（症）

Hemachromatosis is a genetic disorder characterized by the accumulation of iron in various organs.
溢血性铁过载症是一种遗传性疾病，特征是体内多种器官内铁质过多积累。
Early diagnosis and treatment of hemachromatosis are crucial to prevent complications.
对溢血性铁过载症的早期诊断和治疗对于防止并发症至关重要。
Genetic testing is often performed to identify individuals at risk for developing hemachromatosis.
通常会进行基因检测以识别可能发展溢血性铁过载症的人群。
The liver is the primary target organ affected by hemachromatosis, leading to cirrhosis over time.
肝脏是溢血性铁过载症的主要受影响器官，长期会导致肝硬化。
Regular phlebotomies are recommended for patients with hemachromatosis to manage excess iron levels.
对于溢血性铁过载症患者，定期抽血是控制过多铁质水平的常规建议。
Symptoms of hemachromatosis can include fatigue, joint pain, and jaundice.
溢血性铁过载症的症状可能包括疲劳、关节疼痛和黄疸。
In severe cases, hemachromatosis can lead to heart problems and diabetes.
在严重情况下，溢血性铁过载症可能导致心脏问题和糖尿病。
Family members of someone with hemochromatosis should also be screened, as it's an inherited condition.
溢血性铁过载症患者的家族成员也应接受筛查，因为它是一种遗传性疾病。
Treatment for hemachromatosis aims to remove excess iron through bloodletting or medications.
溢血性铁过载症的治疗方法旨在通过放血或药物去除过多的铁。
Long-term management of hemachromatosis requires close monitoring and medical support.
溢血性铁过载症的长期管理需要密切监控和医疗支持。