Conditions / Syndrome
primary ciliary dyskinesia 5
info · Syndrome · ICD-10: Q34.8
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with early onset of a progressive decline in lung function and has_material_basis_in homozygous mutation in the HYDIN gene on chromosome 16q22.
Signs and symptoms
- Chronic rhinitis
- Bronchiectasis
- Bronchial wall thickening
- Reduced sperm motility
- Recurrent sinusitis
- Ciliary dyskinesia
- Recurrent otitis media
- Respiratory failure
- Chronic bronchitis
- Neonatal respiratory distress
Also known as: CILD5; primary ciliary dyskinesia 5 without situs inversus