Williams-Campbell syndrome

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Williams-Campbell syndrome

ORPHA:411501Morphological anomaly

What it is

A rare, respiratory malformation characterized by defective or completely absent bronchial wall cartilage in subsegmental bronchi, leading to distal airway collapse and contributing to the formation of bronchiectasis. The defect is mostly present between the fourth and sixth order bronchial divisions. Clinical manifestation includes recurrent pneumonia, coughing and wheezing.

Key facts

Age of onset
Adult, Childhood
Inheritance
Not applicable
Classified as
Morphological anomaly

ICD-10 codes

Q32.2filed under a broader ICD-10 category

Cross-references

MONDO 0008888UMLS C0340231

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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