n.缺转铁（球）蛋白血症；无铁传递蛋白血

A transferrinemia is a rare genetic disorder characterized by abnormally high levels of transferrin in the blood.
过渡铁蛋白血症是一种罕见的遗传性疾病，其特征是血液中转铁蛋白水平异常升高。
The diagnosis of transferrinemia often involves a complete blood count and iron studies.
诊断过度铁蛋白血症通常包括全面的血液计数和铁代谢检查。
Children with transferrinemia may exhibit symptoms such as jaundice, liver enlargement, and anemia.
患有过度铁蛋白血症的儿童可能出现黄疸、肝脏肿大和贫血等症状。
Treatment for transferrinemia often focuses on reducing iron overload through chelation therapy or phlebotomy.
对于过度铁蛋白血症的治疗常常侧重于通过螯合疗法或抽血来减少铁负荷过重。
Genetic counseling is essential for families with a history of transferrinemia to prevent recurrence.
对于有过度铁蛋白血症家族史的家庭，遗传咨询至关重要，以防止疾病复发。
In transferrinemia, elevated transferrin levels can lead to iron accumulation in various organs, posing health risks.
在过度铁蛋白血症中，升高的转铁蛋白水平可能导致各种器官内铁的积聚，构成健康威胁。
Research is ongoing to develop more effective treatments for transferrinemia, including gene therapy.
目前正在进行研究，以开发更有效的过度铁蛋白血症治疗方法，如基因疗法。
Regular monitoring of iron levels and ferritin levels is crucial for managing transferrinemia.
对铁含量和铁蛋白水平的定期监测对于管理过度铁蛋白血症至关重要。
The severity of transferrinemia varies among individuals, making personalized treatment plans necessary.
过度铁蛋白血症的症状严重程度因人而异，因此需要制定个性化的治疗方案。
Early detection and intervention are vital in preventing complications associated with transferrinemia.
早期发现和干预对于防止与过度铁蛋白血症相关的并发症至关重要。