Pulmonology · Pulmonology / Airway disease
Williams–Campbell syndrome
also: Bronchial cartilage deficiency
Congenital deficiency of subsegmental bronchial cartilage.
- Specialty
- Pulmonology
- Subspecialty
- Pulmonology / Airway disease
- Sex & age distribution
- Male: affected; Female: affected; Children: yes, infancy or childhood
- Gene(s) involved
- None recorded
- Alternative names & eponyms
- Bronchial cartilage deficiency
Etiology & mechanism
Absent cartilage in fourth to sixth bronchial generations.
Gene(s) involved (0)
No gene recorded for this syndrome.
Symptoms & signs (5)
In plain terms, someone with Williams–Campbell 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.
Drag nodes, scroll to zoom, click a node to open that syndrome.
Shares symptoms with
1 shared
Acute chest syndrome
cough
1 shared
Caplan syndrome
cough
1 shared
Carcinoid heart disease
wheezing
1 shared
Carcinoid syndrome
wheezing
1 shared
Hamman–Rich syndrome
cough
1 shared
Hantavirus pulmonary syndrome
cough
1 shared
Heiner syndrome
recurrent pneumonia
1 shared
Hughes–Stovin syndrome
cough
1 shared
Hypereosinophilic syndrome
cough
1 shared
Katayama syndrome
cough
Shares genes with
None.
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