mucoviscidosis diagnosis
粘液纤维化症诊断
treating mucoviscidosis
治疗粘液纤维化症
mucoviscidosis patient
粘液纤维化症患者
mucoviscidosis symptoms
粘液纤维化症症状
cystic mucoviscidosis
囊性纤维化
severe mucoviscidosis
重度粘液纤维化症
mucoviscidosis carrier
粘液纤维化症携带者
childhood mucoviscidosis
儿童粘液纤维化症
advanced mucoviscidosis
晚期粘液纤维化症
mucoviscidosis screening
粘液纤维化症筛查
many children with mucoviscidosis require daily respiratory therapy to maintain lung function.
许多患有囊性纤维化的小孩需要每天进行呼吸治疗以维持肺功能。
early diagnosis of mucoviscidosis significantly improves the quality of life for affected patients.
早期诊断囊性纤维化可以显著提高受影响患者的生活质量。
the genetic mutation responsible for mucoviscidosis affects the cftr protein production.
导致囊性纤维化的基因突变影响CFTR蛋白的产生。
families with a history of mucoviscidosis should consider genetic counseling before planning pregnancy.
有囊性纤维化家族史的家庭在计划怀孕之前应考虑遗传咨询。
advances in medication have extended the life expectancy for individuals living with mucoviscidosis.
药物的进步延长了患有囊性纤维化的人的预期寿命。
regular exercise is recommended as part of the treatment plan for mucoviscidosis patients.
定期锻炼是囊性纤维化患者治疗计划的一部分，建议进行锻炼。
the thick mucus caused by mucoviscidosis can lead to serious respiratory infections.
囊性纤维化引起的浓痰可能导致严重的呼吸道感染。
newborn screening programs help detect mucoviscidosis within the first weeks of life.
新生儿筛查计划有助于在生命最初几个星期内检测出囊性纤维化。
pancreatic insufficiency is a common complication of mucoviscidosis that requires enzyme supplementation.
胰腺功能不全是囊性纤维化的一种常见并发症，需要补充酶。
physiotherapy techniques help clear mucus from the lungs of mucoviscidosis patients.
物理治疗技术有助于清除囊性纤维化患者肺部的粘液。
airborne precautions are essential when treating mucoviscidosis patients with contagious infections.
在治疗患有传染性感染的囊性纤维化患者时，采取空气传播预防措施至关重要。
mucoviscidosis research has led to the development of targeted therapies for the underlying genetic defect.
囊性纤维化研究导致了针对潜在遗传缺陷的靶向治疗的发展。
mucoviscidosis diagnosis
粘液纤维化症诊断
treating mucoviscidosis
治疗粘液纤维化症
mucoviscidosis patient
粘液纤维化症患者
mucoviscidosis symptoms
粘液纤维化症症状
cystic mucoviscidosis
囊性纤维化
severe mucoviscidosis
重度粘液纤维化症
mucoviscidosis carrier
粘液纤维化症携带者
childhood mucoviscidosis
儿童粘液纤维化症
advanced mucoviscidosis
晚期粘液纤维化症
mucoviscidosis screening
粘液纤维化症筛查
many children with mucoviscidosis require daily respiratory therapy to maintain lung function.
许多患有囊性纤维化的小孩需要每天进行呼吸治疗以维持肺功能。
early diagnosis of mucoviscidosis significantly improves the quality of life for affected patients.
早期诊断囊性纤维化可以显著提高受影响患者的生活质量。
the genetic mutation responsible for mucoviscidosis affects the cftr protein production.
导致囊性纤维化的基因突变影响CFTR蛋白的产生。
families with a history of mucoviscidosis should consider genetic counseling before planning pregnancy.
有囊性纤维化家族史的家庭在计划怀孕之前应考虑遗传咨询。
advances in medication have extended the life expectancy for individuals living with mucoviscidosis.
药物的进步延长了患有囊性纤维化的人的预期寿命。
regular exercise is recommended as part of the treatment plan for mucoviscidosis patients.
定期锻炼是囊性纤维化患者治疗计划的一部分，建议进行锻炼。
the thick mucus caused by mucoviscidosis can lead to serious respiratory infections.
囊性纤维化引起的浓痰可能导致严重的呼吸道感染。
newborn screening programs help detect mucoviscidosis within the first weeks of life.
新生儿筛查计划有助于在生命最初几个星期内检测出囊性纤维化。
pancreatic insufficiency is a common complication of mucoviscidosis that requires enzyme supplementation.
胰腺功能不全是囊性纤维化的一种常见并发症，需要补充酶。
physiotherapy techniques help clear mucus from the lungs of mucoviscidosis patients.
物理治疗技术有助于清除囊性纤维化患者肺部的粘液。
airborne precautions are essential when treating mucoviscidosis patients with contagious infections.
在治疗患有传染性感染的囊性纤维化患者时，采取空气传播预防措施至关重要。
mucoviscidosis research has led to the development of targeted therapies for the underlying genetic defect.
囊性纤维化研究导致了针对潜在遗传缺陷的靶向治疗的发展。
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