Add to ORKGPrimary ciliary dyskinesia(PCD) is a congenital disorder of cilia mostly associated with ultrastructural defects and resulting in immotility or abnormal motility, with or without a situs inversus. The defects of cilia in PCD cause chronic or recurrent upper and lower respiratory diseases, such as chronic bronchitis, bronchiectasis, chronic sinusitis and otitis media with effusion. Transmission electron microscopy of sperm or respiratory ciliated mucosa allows specific anatomic diagnosis of PCD. Treatment is symptomatic and directed against complications in the respiratory tract. Early physiotherapy is recommended
Primary ciliary dyskinesia (PCD) is a multi-organ disorder associated with chronic oto-sino-pulmonar...
Primary ciliary dyskinesia (PCD) is an inherited autosomal-recessive disorder of motile cilia charac...
Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous disease, characterized by cili...
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...
Primary ciliary dyskinesia (PCD) is associated with abnormal ciliary structure and function, which r...
Primary ciliary dyskinesia (PCD) is a genetic disorder of ciliary structure or function. It results ...
Primary ciliary dyskinesia (PCD) is an inherited cause of bronchiectasis. The estimated PCD prevalen...
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...
Summary Primary ciliary dyskinesia (PCD) is a genetic disorder of cilia structure and function, chro...
Primary Ciliary Dyskinesia (PCD) is a rare congenital, clinically and genetically heterogeneous dise...
Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disease, caused by specific primary s...
Primary ciliary dyskinesia (PCD) is a multi-organ disorder associated with chronic oto-sino-pulmonar...
Primary ciliary dyskinesia (PCD) is an inherited autosomal-recessive disorder of motile cilia charac...
Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous disease, characterized by cili...
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...
Primary ciliary dyskinesia (PCD) is associated with abnormal ciliary structure and function, which r...
Primary ciliary dyskinesia (PCD) is a genetic disorder of ciliary structure or function. It results ...
Primary ciliary dyskinesia (PCD) is an inherited cause of bronchiectasis. The estimated PCD prevalen...
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...
Summary Primary ciliary dyskinesia (PCD) is a genetic disorder of cilia structure and function, chro...
Primary Ciliary Dyskinesia (PCD) is a rare congenital, clinically and genetically heterogeneous dise...
Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disease, caused by specific primary s...
Primary ciliary dyskinesia (PCD) is a multi-organ disorder associated with chronic oto-sino-pulmonar...
Primary ciliary dyskinesia (PCD) is an inherited autosomal-recessive disorder of motile cilia charac...
Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous disease, characterized by cili...