酪氨酸血症

Tyrosinemia type 1 is a rare genetic disorder that impairs the body's ability to break down a substance called tyrosine.
酪氨酸症是一种罕见的遗传病，它阻碍身体分解名为酪氨酸的物质。
The child was diagnosed with tyrosinemia, necessitating a strict dietary restriction to manage her symptoms.
这个孩子被诊断为酪氨酸症，需要严格的饮食限制来控制症状。
Tyrosinemia patients often exhibit darkening of their skin and hair due to excess tyrosine buildup.
酪氨酸症患者由于酪氨酸堆积，皮肤和头发常常会变黑。
Scientists are researching new treatments for tyrosinemia type 2, which affects the liver.
科学家们正在研究针对2型酪氨酸症的新治疗方法，这种病症影响肝脏。
A clinical trial is underway to test a new enzyme replacement therapy for tyrosinemia patients.
一项临床试验正在进行中，目的是测试对酪氨酸症患者的新型酶替代疗法。
Tyrosinemia type 3, also known as phenylketonuria, is caused by a deficiency in an enzyme in the brain.
酪氨酸症，又称苯丙酮尿症，是由于大脑中一种酶的缺乏引起的。
Prevention involves监视 newborns for early detection and treatment of tyrosinemia cases.
预防措施包括对新生儿进行早期检测和治疗，以防止酪氨酸症的发生。
The organization provides support groups and educational resources for individuals with tyrosinemia and their families.
该组织为酪氨酸症患者及其家庭提供支持团体和教育资源。
Tyrosine levels in the blood can be measured through regular genetic testing for early diagnosis.
通过定期的基因检测可以测量血液中的酪氨酸水平，以便早做诊断。
Advancements in gene therapy hold promise for someday curing tyrosinemia altogether.
基因疗法的进步为将来彻底治愈酪氨酸症带来了希望。