International audiencePrimary ciliary dyskinesia (PCD) is a rare inherited ciliopathy in which respiratory cilia are stationary or dyskinetic. The clinical presentation of PCD is highly non-specific since it includes infections and disorders of the upper (otitis and rhinosinusitis) and lower (neonatal respiratory distress, bronchitis, pneumonia and bronchiectasis) airways, starting in early life. Clinical examination alone does not allow a PCD diagnosis, which relies on several concordant tests, since none are sensitive or specific enough alone. Despite being the most sensitive and specific test to diagnose PCD, digital high-speed videomicroscopy (DHSV) is not sufficiently standardized, preventing its use with complete confidence as a confi...
The diagnosis of primary ciliary dyskinesia is often confirmed with standard, albeit complex and exp...
Primary ciliary dyskinesia (PCD) is a rare congenital respiratory disorder characterized by abnormal...
Background: Primary ciliary dyskinesia (PCD) is a rare congenital respiratory disorder characterized...
International audiencePrimary ciliary dyskinesia (PCD) is a rare inherited ciliopathy in which respi...
Key points Primary ciliary dyskinesia (PCD) is a genetically and clinically heterogeneous disease ch...
The diagnosis of primary ciliary dyskinesia is often confirmed with standard, albeit complex and exp...
Primary ciliary dyskinesia (PCD) is a rare genetic disease characterized by dyskinetic cilia. Respir...
International audiencePrimary ciliary dyskinesia (PCD) is a rare congenital respiratory disorder cha...
Primary ciliary dyskinesia is a rare heterogeneous recessive genetic disorder of motile cilia, leadi...
Primary ciliary dyskinesia (PCD) is a rare, heterogeneous, recessive, genetic disorder of motile cil...
The diagnosis of primary ciliary dyskinesia is often confirmed with standard, albeit complex and exp...
Primary ciliary dyskinesia (PCD) is a rare congenital respiratory disorder characterized by abnormal...
Background: Primary ciliary dyskinesia (PCD) is a rare congenital respiratory disorder characterized...
International audiencePrimary ciliary dyskinesia (PCD) is a rare inherited ciliopathy in which respi...
Key points Primary ciliary dyskinesia (PCD) is a genetically and clinically heterogeneous disease ch...
The diagnosis of primary ciliary dyskinesia is often confirmed with standard, albeit complex and exp...
Primary ciliary dyskinesia (PCD) is a rare genetic disease characterized by dyskinetic cilia. Respir...
International audiencePrimary ciliary dyskinesia (PCD) is a rare congenital respiratory disorder cha...
Primary ciliary dyskinesia is a rare heterogeneous recessive genetic disorder of motile cilia, leadi...
Primary ciliary dyskinesia (PCD) is a rare, heterogeneous, recessive, genetic disorder of motile cil...
The diagnosis of primary ciliary dyskinesia is often confirmed with standard, albeit complex and exp...
Primary ciliary dyskinesia (PCD) is a rare congenital respiratory disorder characterized by abnormal...
Background: Primary ciliary dyskinesia (PCD) is a rare congenital respiratory disorder characterized...