Phenylketonuria is a genetic disorder that affects how the body processes protein.
苯丙酮尿症是一种影响身体如何处理蛋白质的遗传性疾病。
Individuals with phenylketonuria need to follow a strict low-protein diet.
患有苯丙酮尿症的个体需要遵循严格的低蛋白饮食。
Newborn screening can detect phenylketonuria early so that treatment can begin promptly.
新生儿筛查可以早期检测苯丙酮尿症，以便及时开始治疗。
Phenylketonuria can lead to intellectual disabilities if not managed properly.
苯丙酮尿症如果没有得到适当管理可能会导致智力障碍。
The phenylketonuria test involves a blood sample to measure phenylalanine levels.
苯丙酮尿症测试涉及抽取血样以测量苯丙氨酸水平。
Dietary supplements may be recommended for individuals with phenylketonuria to meet their nutritional needs.
可能会建议患有苯丙酮尿症的个体服用膳食补充剂以满足其营养需求。
Parents of children with phenylketonuria often need to work closely with healthcare providers to manage the condition.
患有苯丙酮尿症的儿童的父母通常需要与医疗服务提供者密切合作以管理该疾病。
Phenylketonuria is a rare disorder, affecting about 1 in every 10,000 to 15,000 newborns.
苯丙酮尿症是一种罕见的疾病，大约每1万到1.5万名新生儿中有1名受影响。
Regular monitoring of phenylalanine levels is essential for individuals with phenylketonuria.
定期监测苯丙氨酸水平对患有苯丙酮尿症的个体至关重要。
Phenylketonuria is typically diagnosed through newborn screening tests shortly after birth.
苯丙酮尿症通常是通过新生儿筛查测试在出生后不久被诊断出的。
Phenylketonuria is a genetic disorder that affects how the body processes protein.
苯丙酮尿症是一种影响身体如何处理蛋白质的遗传性疾病。
Individuals with phenylketonuria need to follow a strict low-protein diet.
患有苯丙酮尿症的个体需要遵循严格的低蛋白饮食。
Newborn screening can detect phenylketonuria early so that treatment can begin promptly.
新生儿筛查可以早期检测苯丙酮尿症，以便及时开始治疗。
Phenylketonuria can lead to intellectual disabilities if not managed properly.
苯丙酮尿症如果没有得到适当管理可能会导致智力障碍。
The phenylketonuria test involves a blood sample to measure phenylalanine levels.
苯丙酮尿症测试涉及抽取血样以测量苯丙氨酸水平。
Dietary supplements may be recommended for individuals with phenylketonuria to meet their nutritional needs.
可能会建议患有苯丙酮尿症的个体服用膳食补充剂以满足其营养需求。
Parents of children with phenylketonuria often need to work closely with healthcare providers to manage the condition.
患有苯丙酮尿症的儿童的父母通常需要与医疗服务提供者密切合作以管理该疾病。
Phenylketonuria is a rare disorder, affecting about 1 in every 10,000 to 15,000 newborns.
苯丙酮尿症是一种罕见的疾病，大约每1万到1.5万名新生儿中有1名受影响。
Regular monitoring of phenylalanine levels is essential for individuals with phenylketonuria.
定期监测苯丙氨酸水平对患有苯丙酮尿症的个体至关重要。
Phenylketonuria is typically diagnosed through newborn screening tests shortly after birth.
苯丙酮尿症通常是通过新生儿筛查测试在出生后不久被诊断出的。
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