Understanding Primary ciliary dyskinesia 26
By Dr. Hassan Yamamoto, MD · · Genetic Medicine
Our Genetic Medicine team put together this overview of primary ciliary dyskinesia 26 for patients and families.
About this topic
Topic: primary ciliary dyskinesia 26. A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner and outer dynein arm defect, neonatal respiratory distress, recurrent upper and lower airway disease, bronchiectasis, and variable occurence of laterality defects and has_material_basis_in homozygous or compound heterozygous mutation in the C21ORF59 gene on chromosome 21q22.
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This article is for general information and does not replace advice from your clinician.