Phenylketonuria is a genetic disorder that affects how the body processes protein.
苯丙酮尿症是一種影響身體如何處理蛋白質的遺傳性疾病。
Individuals with phenylketonuria need to follow a strict low-protein diet.
患有苯丙酮尿症的個體需要遵循嚴格的低蛋白飲食。
Newborn screening can detect phenylketonuria early so that treatment can begin promptly.
新生兒篩查可以早期檢測苯丙酮尿症，以便及時開始治療。
Phenylketonuria can lead to intellectual disabilities if not managed properly.
苯丙酮尿症如果沒有得到適當管理可能會導致智力障礙。
The phenylketonuria test involves a blood sample to measure phenylalanine levels.
苯丙酮尿症測試涉及抽取血樣以測量苯丙氨酸水平。
Dietary supplements may be recommended for individuals with phenylketonuria to meet their nutritional needs.
可能會建議患有苯丙酮尿症的個體服用膳食補充劑以滿足其營養需求。
Parents of children with phenylketonuria often need to work closely with healthcare providers to manage the condition.
患有苯丙酮尿症的兒童的父母通常需要與醫療服務提供者密切合作以管理該疾病。
Phenylketonuria is a rare disorder, affecting about 1 in every 10,000 to 15,000 newborns.
苯丙酮尿症是一種罕見的疾病，大約每1萬到1.5萬名新生兒中有1名受影響。
Regular monitoring of phenylalanine levels is essential for individuals with phenylketonuria.
定期監測苯丙氨酸水平對患有苯丙酮尿症的個體至關重要。
Phenylketonuria is typically diagnosed through newborn screening tests shortly after birth.
苯丙酮尿症通常是通過新生兒篩查測試在出生後不久被診斷出的。
Phenylketonuria is a genetic disorder that affects how the body processes protein.
苯丙酮尿症是一種影響身體如何處理蛋白質的遺傳性疾病。
Individuals with phenylketonuria need to follow a strict low-protein diet.
患有苯丙酮尿症的個體需要遵循嚴格的低蛋白飲食。
Newborn screening can detect phenylketonuria early so that treatment can begin promptly.
新生兒篩查可以早期檢測苯丙酮尿症，以便及時開始治療。
Phenylketonuria can lead to intellectual disabilities if not managed properly.
苯丙酮尿症如果沒有得到適當管理可能會導致智力障礙。
The phenylketonuria test involves a blood sample to measure phenylalanine levels.
苯丙酮尿症測試涉及抽取血樣以測量苯丙氨酸水平。
Dietary supplements may be recommended for individuals with phenylketonuria to meet their nutritional needs.
可能會建議患有苯丙酮尿症的個體服用膳食補充劑以滿足其營養需求。
Parents of children with phenylketonuria often need to work closely with healthcare providers to manage the condition.
患有苯丙酮尿症的兒童的父母通常需要與醫療服務提供者密切合作以管理該疾病。
Phenylketonuria is a rare disorder, affecting about 1 in every 10,000 to 15,000 newborns.
苯丙酮尿症是一種罕見的疾病，大約每1萬到1.5萬名新生兒中有1名受影響。
Regular monitoring of phenylalanine levels is essential for individuals with phenylketonuria.
定期監測苯丙氨酸水平對患有苯丙酮尿症的個體至關重要。
Phenylketonuria is typically diagnosed through newborn screening tests shortly after birth.
苯丙酮尿症通常是通過新生兒篩查測試在出生後不久被診斷出的。
探索常見搜尋詞彙