Primary ciliary dyskinesia (PCD) is a rare genetic disease which affects one person in 20,000. The disease is characterised by motility defects in cellular micro-cilia.

Indiana University School of Medicine researchers have uncovered compelling evidence that children with primary ciliary dyskinesia (PCD), a rare genetic disorder affecting airway function, are ...

Primary ciliary dyskinesia (PCD) is a congenital disorder of children, caused by a variety of genetic mutations. It is thus a heterogeneous disorder, with the same clinical manifestations being ...

Primary ciliary dyskinesia (PCD) is a rare genetic disease characterized by deficient mucociliary clearance (MCC), chronic respiratory tract infections, bronchiectasis, and declining respiratory ...

Researchers have uncovered compelling evidence that children with primary ciliary dyskinesia (PCD), a rare genetic disorder affecting airway function, are significantly more likely than children ...

AIIMS Delhi scientists developed India’s first TEM-based method to diagnose rare genetic disorder PCD, boosting accuracy and detecting ciliary defects in 70% of suspected cases, enabling early ...

Kartagener syndrome is a rare genetic disease that affects the cilia in your lungs and other organs. What Is Kartagener Syndrome? Kartagener syndrome is a type of primary ciliary dyskinesia or PCD ...

Cedars-Sinai investigators have identified a genetic variant that increases people’s risk of developing perianal Crohn’s disease (pCD), the most debilitating manifestation of the inflammatory ...

The funding will also allow ReCode to advance its PCD and CF programs into the clinic, and further develop its genetic medicine delivery platform to deliver additional treatments—from gene ...

A Midlothian woman has been identified as only one of 12 people in the world to carry a newly discovered genetic mutation linked to the development of a rare and incurable lung disease.. Bailey ...