Conditions / Syndrome
primary ciliary dyskinesia 7
info · Syndrome · ICD-10: Q34.8
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with chronic respiratory infections, chronic sinusitis, recurrent bronchitis, and pneumonia beginning in infancy or early childhood and has_material_basis_in mutation in the
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with chronic respiratory infections, chronic sinusitis, recurrent bronchitis, and pneumonia beginning in infancy or early childhood and has_material_basis_in mutation in the DNAH11 gene on chromosome 7p21.
Signs and symptoms
- Chronic rhinitis
- Dextrocardia
- Bronchiectasis
- Decreased nasal nitric oxide
- Cough
- Ciliary dyskinesia
- Abnormal ciliary motility
- Recurrent otitis media
- Recurrent pneumonia
- Restrictive ventilatory defect
Also known as: CILD7; primary ciliary dyskinesia 7 with or without situs inversus