Primary ciliary dyskinesia (PCD) (MIM no. 244400) is a genetically heterogeneous, typically autosomal recessive, disorder characterized by ciliary dysfunction and impaired mucociliary clearance ...

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 ...

Kartagener syndrome is a type of primary ciliary dyskinesia or PCD, that may also cause reversed internal organs. This means your organs are on the opposite side of your body from where they ...

We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. Patients classified as likely having primary ciliary ...

“Establishing TEM-based diagnosis using this method may be helpful for the proper treatment of PCD with appropriate clinical guidelines,” said the study. A rare genetic disorder, PCD is ...

We believe this new online tool will advance our understanding of this rare disorder, help us recruit candidates for research studies and ultimately improve care for PCD patients. "We will ...

Researchers said understanding the overlap between primary ciliary dyskinesia and asthma is critical to helping young patients have healthier respiratory outcomes. INDIANAPOLIS — Indiana ...

Validated on 200 patients with suspected ciliary disorders, the technique confirmed diagnoses in 135 cases. The scope of this technique extends far beyond PCD. It can accurately detect a range of ...

As PCD is a multi-system disorder requiring multi-disciplinary care, (including respiratory management, Ear, Nose and Throat (ENT), cardiology, dietetics, and fertility input), earlier diagnosis ...

or PCD, a rare and often misdiagnosed genetic disorder affecting the respiratory system. The innovative technique, built around transmission electron microscopy, or TEM, stands to revolutionise ...