primary ciliary dyskinesia 10

A primary ciliary dyskinesia that is characterized by outer and inner dynein arm absence, chronic otitis media, sinusitis, recurrent pneumonia and variable occurrence of situs inversus and has_material_basis_in homozygous mutation in the KTU gene on chromosome

A primary ciliary dyskinesia that is characterized by outer and inner dynein arm absence, chronic otitis media, sinusitis, recurrent pneumonia and variable occurrence of situs inversus and has_material_basis_in homozygous mutation in the KTU gene on chromosome 14q21.

Signs and symptoms

• Chronic otitis media
• Chronic sinusitis
• Situs inversus totalis
• Ciliary dyskinesia
• Abnormal respiratory motile cilium morphology
• Recurrent sinusitis

Also known as: CILD10; primary ciliary dyskinesia 10 with or without situs inversus