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原发性纤毛运动障碍:诊断年龄及症状史

Primary ciliary dyskinesia: age at diagnosis and symptom history.

作者信息

Coren M E, Meeks M, Morrison I, Buchdahl R M, Bush A

机构信息

Department of Paediatric Respiratory Medicine, Royal Brompton Hospital, London, UK.

出版信息

Acta Paediatr. 2002;91(6):667-9. doi: 10.1080/080352502760069089.

Abstract

UNLABELLED

Age at diagnosis and the symptom history of children with primary ciliary dyskinesia (PCD) are described by reviewing the case notes in the paediatric PCD clinic. Mean age at diagnosis was 4.4 y despite a history of neonatal respiratory distress in 37/55 cases, situs inversus in 38/55 cases and early onset troublesome rhinitis in 42/55.

CONCLUSION

Diagnosis of PCD is often delayed despite the presence of typical symptoms early in life. The key clinical features of unexplained neonatal respiratory distress, early onset rhinitis, situs inversus and a productive cough are highlighted, which, especially when occurring in combination, makes early referral for specific testing for PCD mandatory.

摘要

未标注

通过回顾儿科原发性纤毛运动障碍(PCD)诊所的病例记录,描述了PCD患儿的诊断年龄和症状史。尽管55例中有37例有新生儿呼吸窘迫史、55例中有38例有内脏反位、55例中有42例有早发性难治性鼻炎,但诊断时的平均年龄为4.4岁。

结论

尽管在生命早期存在典型症状,但PCD的诊断往往延迟。强调了不明原因的新生儿呼吸窘迫、早发性鼻炎、内脏反位和咳痰性咳嗽等关键临床特征,这些特征尤其是同时出现时,使得必须尽早转诊以进行PCD的特异性检测。

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