Ciliary dyskinesia (Q42980): Difference between revisions
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Função defeituosa dos cílios revestindo o trato respiratório (inferior e superior, seios, tuba auditiva, orelha média) resultando em transporte mucociliar alterado e se manifestando como como infecção recorrente de vias aéreas superiores e inferiores, tosse crônica produtiva, rinossinusite crônica ou otite média persistente. As forma adquiridas resultam de lesão do trato respiratório associada principalmente a infecções como bronquiolites ou doença pulmonar obstrutiva crônica. As raras formas primárias são herdadas como transtorno autossômico recessivo que se apresenta precocemente na vida e tipicamente progridem para bronquiectasias; podem estar associadas a infertilidade no homem e na mulher, devido a mobilidade anormal dos espermatozoides ou da função alterada das tubas uterinas, respectivamente. | |||
| description / en | description / en | ||
Defective function of the cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube, middle ear) resulting in altered mucociliary transport and manifesting as recurrent upper and lower respiratory infection, chronic productive cough, chronic rhinosinusitis or persistent otitis media. Acquired forms result from respiratory tract injury associated especially with respiratory infections such as bronchiolitis or chronic obstructive pulmonary disease. The rare primary forms are inherited as autosomal recessive disorders presenting early in life and typically progressing to bronchiectasis; they may be associated with infertility in men and women due to abnormal sperm motility or fallopian tube function respectively. | |||
Revision as of 09:45, 13 August 2026
Defective function of the cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube, middle ear) resulting in altered mucociliary transport and manifesting as recurrent upper and lower respiratory infection, chronic productive cough, chronic rhinosinusitis or persistent otitis media. Acquired forms result from respiratory tract injury associated especially with respiratory infections such as bronchiolitis or chronic obstructive pulmonary disease. The rare primary forms are inherited as autosomal recessive disorders presenting early in life and typically progressing to bronchiectasis; they may be associated with infertility in men and women due to abnormal sperm motility or fallopian tube function respectively.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | CB40.0 |
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| English | Ciliary dyskinesia |
Defective function of the cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube, middle ear) resulting in altered mucociliary transport and manifesting as recurrent upper and lower respiratory infection, chronic productive cough, chronic rhinosinusitis or persistent otitis media. Acquired forms result from respiratory tract injury associated especially with respiratory infections such as bronchiolitis or chronic obstructive pulmonary disease. The rare primary forms are inherited as autosomal recessive disorders presenting early in life and typically progressing to bronchiectasis; they may be associated with infertility in men and women due to abnormal sperm motility or fallopian tube function respectively. |
