Marked tracheal and main bronchial dilation.
- Specialty
- Pulmonology
- Subspecialty
- Pulmonology / Airway disease
- Sex & age distribution
- Male: affected, 8:1 male predominance; Female: affected; Children: rare
- Gene(s) involved
- None recorded
- Alternative names & eponyms
- Tracheobronchomegaly
Etiology & mechanism
Elastic and smooth muscle atrophy of tracheal wall.
Gene(s) involved (0)
No gene recorded for this syndrome.
Symptoms & signs (5)
In plain terms, someone with Mounier-Kuhn syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
3 shared
Lady Windermere syndrome
bronchiectasis, chronic cough, hemoptysis
2 shared
Eisenmenger syndrome
dyspnea, hemoptysis
2 shared
Goodpasture syndrome
dyspnea, hemoptysis
2 shared
Hughes–Stovin syndrome
dyspnea, hemoptysis
2 shared
Kartagener syndrome
bronchiectasis, chronic cough
2 shared
Pulmonary–renal syndrome
dyspnea, hemoptysis
2 shared
Yellow nail syndrome
bronchiectasis, chronic cough
1 shared
Caplan syndrome
dyspnea
1 shared
Cardiorenal syndrome
dyspnea
1 shared
Chilaiditi syndrome
dyspnea
Shares genes with
None.
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