Living With Primary ciliary dyskinesia 17
By Dr. Lucas Murphy, MD · · Genetic Medicine
Patients often ask us about primary ciliary dyskinesia 17. Here is what our Genetic Medicine clinicians want you to know.
About this topic
Topic: primary ciliary dyskinesia 17. A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner and outer dynein arm defect, early infantile onset of respiratory distress, and variable occurence of laterality defects and has_material_basis_in homozygous mutation in the CCDC103 gene on chromosome 17q21.
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This article is for general information and does not replace advice from your clinician.