Add to ORKGSummary Primary ciliary dyskinesia (PCD) is a genetic disorder of cilia structure and function, chronic infections of the respiratory tract, fertility problems and disorders of organ laterality. Establishing a definitive diagnosis can be challenging, requiring a compatible phenotype and detection of ciliary functional and ultra-structural defects, along with newer screening tools such as nasal nitric oxide and genetics testing. 10 known PCDcausing mutations within two genes are now available in a clinical panel, and in the future, comprehensive genetic testing may serve to identify young infants with PCD to improve the long-term outlook for patients with the disease. Therapy includes regular pulmonary function testing and monitoring of sput...
Primary ciliary dyskinesia (PCD) is usually inherited as an autosomal recessive, and in classical fo...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disease, caused by specific primary s...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary ciliary dyskinesia (PCD) is an inherited cause of bronchiectasis. The estimated PCD prevalen...
Primary ciliary dyskinesia (PCD) is an inherited autosomal-recessive disorder of motile cilia charac...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure and function,...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure, function, an...
Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous disease, characterized by cili...
Primary Ciliary Dyskinesia (PCD) is a rare congenital, clinically and genetically heterogeneous dise...
Primary ciliary dyskinesia (PCD) is a congenital, clinically and ultrastructurally heterogeneous dis...
Primary ciliary dyskinesia (PCD) is usually inherited as an autosomal recessive, and in classical fo...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disease, caused by specific primary s...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary ciliary dyskinesia (PCD) is an inherited cause of bronchiectasis. The estimated PCD prevalen...
Primary ciliary dyskinesia (PCD) is an inherited autosomal-recessive disorder of motile cilia charac...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure and function,...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder of cilia structure, function, an...
Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous disease, characterized by cili...
Primary Ciliary Dyskinesia (PCD) is a rare congenital, clinically and genetically heterogeneous dise...
Primary ciliary dyskinesia (PCD) is a congenital, clinically and ultrastructurally heterogeneous dis...
Primary ciliary dyskinesia (PCD) is usually inherited as an autosomal recessive, and in classical fo...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disease, caused by specific primary s...