Primary ciliary dyskinesia (PCD) is a genetic disorder of ciliary structure or function. It results in mucus accumulation and bacterial colonization of the respiratory tract which leads to chronic upper and lower airway infections, organ laterality defects, and fertility problems. We review the respiratory signs and symptoms of PCD, as well as the screening tests for and diagnostic investigation of the disease, together with details related to ciliary function, ciliary ultrastructure, and genetic studies. In addition, we describe the difficulties in diagnosing PCD by means of transmission electron microscopy, as well as describing patient follow-up procedures
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure, function, an...
Primary ciliary dyskinesia (PCD) is a rare genetic disease characterized by dyskinetic cilia. Respir...
Primary Ciliary Dyskinesia (PCD) is a rare congenital, clinically and genetically heterogeneous dise...
Primary ciliary dyskinesia (PCD) is a genetic disorder of ciliary structure or function. It results ...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disease with an incidence estimated betwe...
Primary ciliary dyskinesia (PCD) is associated with abnormal ciliary structure and function, which r...
Summary Primary ciliary dyskinesia (PCD) is a genetic disorder of cilia structure and function, chro...
Primary ciliary dyskinesia (PCD) is an inherited autosomal-recessive disorder of motile cilia charac...
Primary ciliary dyskinesia (PCD) is associated with abnormal ciliary structure and function, which r...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure, function, an...
Primary ciliary dyskinesia (PCD) is a rare genetic disease characterized by dyskinetic cilia. Respir...
Primary Ciliary Dyskinesia (PCD) is a rare congenital, clinically and genetically heterogeneous dise...
Primary ciliary dyskinesia (PCD) is a genetic disorder of ciliary structure or function. It results ...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disease with an incidence estimated betwe...
Primary ciliary dyskinesia (PCD) is associated with abnormal ciliary structure and function, which r...
Summary Primary ciliary dyskinesia (PCD) is a genetic disorder of cilia structure and function, chro...
Primary ciliary dyskinesia (PCD) is an inherited autosomal-recessive disorder of motile cilia charac...
Primary ciliary dyskinesia (PCD) is associated with abnormal ciliary structure and function, which r...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure, function, an...
Primary ciliary dyskinesia (PCD) is a rare genetic disease characterized by dyskinetic cilia. Respir...
Primary Ciliary Dyskinesia (PCD) is a rare congenital, clinically and genetically heterogeneous dise...