Conditions / Syndrome
primary ciliary dyskinesia 35
info · Syndrome
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with absent outer dynein arms, immotile cilia, variable occurence of laterality defects and recurrent upper and lower respiratory infections and has_material_basis_in homozyg
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with absent outer dynein arms, immotile cilia, variable occurence of laterality defects and recurrent upper and lower respiratory infections and has_material_basis_in homozygous mutation in the TTC25 gene on chromosome 17q21.
Signs and symptoms
- Chronic rhinitis
- Bronchiectasis
- Decreased nasal nitric oxide
- Nasal polyposis
- Productive cough
- Chronic sinusitis
- Recurrent pneumonia
- Chronic otitis media
- Situs inversus totalis
- Abdominal situs ambiguus
Also known as: CILD35; primary ciliary dyskinesia 35 with or without situs inversus