phenylketonuria
「phenylketonuria」的意思
n. [泌尿] 苯丙酮尿；[泌尿] 苯丙酮酸尿
n.[医]苯丙酮尿,苯丙酮酸尿症(一种先天性代谢异常)
「phenylketonuria」的用法
phenylketonuria苯酮尿症 - 医学专业术语
「phenylketonuria」的例句
Phenylketonuria is a genetic disorder that affects the body's ability to process phenylalanine.
苯酮尿症是一种遗传性疾病，影响身体处理苯丙氨酸的能力。
The diagnosis of phenylketonuria is typically made through blood tests.
苯酮尿症的诊断通常通过血液检查进行。
Untreated phenylketonuria can lead to severe brain damage in infants and children.
未经治疗的苯酮尿症可能导致婴儿和儿童严重的脑损伤。
Phenylalanine is an essential amino acid that the body cannot produce on its own.
苯丙氨酸是一种人体不能自行生产的必需氨基酸。
Individuals with phenylketonuria must follow a strict diet to manage their condition.
患有苯酮尿症的人必须遵循严格的饮食计划来管理他们的状况。
Symptoms of phenylketonuria can include intellectual disability, seizures, and behavioral problems.
苯酮尿症的症状可能包括智力障碍、癫痫和行为问题。
Phenylalanine is found in many foods, including dairy products, meats, and certain vegetables.
苯丙氨酸存在于许多食物中，包括乳制品、肉类和某些蔬菜。
The treatment for phenylketonuria involves maintaining a low-phenylalanine diet.
苯酮尿症的治疗涉及维持低苯丙氨酸饮食。
Genetic counseling is often recommended for families with a history of phenylketonuria.
对于有苯酮尿症家族史的家庭，通常建议进行遗传咨询。
Regular monitoring of blood levels of phenylalanine is necessary for effective management.
有效管理需要定期监测血液中苯丙氨酸的水平。