Primary ciliary dyskinesia, also known as ciliary immobility syndrome, is an autosomal recessive disorder.
Patients may suffer from a series of clinical disorders caused by abnormal ciliary function, including recurrent respiratory infections, recurrent pneumonia, bronchiectasis, chronic sinusitis, chronic otitis media, etc. They may also suffer from visceral transposition and impact on fertility.
Primary ciliary dyskinesia occurs most often in preschool children and young adults, and the tests required for the disease generally include imaging, electron microscopy, and white blood cell count tests. For the treatment of primary ciliary dyskinesia, anti-infective treatment is the main focus, and appropriate treatment programs are adopted for different diseases.
Therefore, it is recommended that patients go to the hospital for diagnosis and treatment as soon as possible in order to achieve a good prognosis; because primary ciliary dyskinesia has a family genetic tendency, there is an intergenerational or intergenerational incidence, so pregnant women should strengthen the health care during pregnancy, and prohibit consanguineous marriages.