Primary ciliary dyskinesia (PCD) is a multi-organ disorder associated with chronic oto-sino-pulmonary disease, neonatal respiratory distress, situs abnormalities and reduced fertility. Repeated respiratory tract infections leads to the almost universal development of bronchiectasis. These clinical manifestations are a consequence of poorly functioning motile cilia. However, confirming the diagnosis is quite difficult and is often delayed, so the true incidence of PCD may be significantly higher than current estimates. Nasal nitric oxide has been earmarked as a useful screening tool for identifying patients, but its use is limited in pre-school-aged children. Due to the rarity of PCD, the evidence base for management is somewhat limited, and...
Primary ciliary dyskinesia(PCD) is a congenital disorder of cilia mostly associated with ultrastruct...
Primary ciliary dyskinesia (PCD) is usually inherited as an autosomal recessive, and in classical fo...
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 associated with abnormal ciliary structure and function, which r...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary ciliary dyskinesia (PCD) is associated with abnormal ciliary structure and function, which r...
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...
Summary Primary ciliary dyskinesia (PCD) is a genetic disorder of cilia structure and function, chro...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Introduction: Primary ciliary dyskinesia (PCD) is a rare, mostly autosomal-recessive disorder of mot...
Primary ciliary dyskinesia(PCD) is a congenital disorder of cilia mostly associated with ultrastruct...
Primary ciliary dyskinesia (PCD) is usually inherited as an autosomal recessive, and in classical fo...
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 associated with abnormal ciliary structure and function, which r...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Primary ciliary dyskinesia (PCD) is associated with abnormal ciliary structure and function, which r...
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...
Summary Primary ciliary dyskinesia (PCD) is a genetic disorder of cilia structure and function, chro...
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia t...
Introduction: Primary ciliary dyskinesia (PCD) is a rare, mostly autosomal-recessive disorder of mot...
Primary ciliary dyskinesia(PCD) is a congenital disorder of cilia mostly associated with ultrastruct...
Primary ciliary dyskinesia (PCD) is usually inherited as an autosomal recessive, and in classical fo...
Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous disease, characterized by cili...