Two-term infants were diagnosed with Kartagener Syndrome in the immediate neonatal period following presentation with unexplained respiratory distress and situs inversus. This allowed early initiation ...

Please provide your email address to receive an email when new articles are posted on . Elevated sputum inflammation markers were linked to lower lung function in primary ciliary dyskinesia.

Primary ciliary dyskinesia (PCD) is a rare disease of children and was the first human disease linked to cilia dysfunction. Nearly four decades have passed since the disease was linked to ...

DelveInsight’s, “Primary Ciliary Dyskinesia – Pipeline Insight, 2025,” report provides comprehensive insights about 4+ companies and 4+ pipeline drugs in Primary Ciliary Dyskinesia pipeline landscape.

Lung, cilary dyskinesia Recent guidelines set forth by an interdisciplinary panel assembled by the American Thoracic Society sought to demystify primary ciliary dyskinesia and address 4 main ...

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 ...

MENLO PARK, Calif. & DALLAS--(BUSINESS WIRE)--ReCode Therapeutics (the “Company”), a biopharmaceutical company pioneering disease-modifying genetic medicines using its proprietary LNP delivery ...

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

LEXINGTON, Mass., May 18, 2021 (GLOBE NEWSWIRE) -- Translate Bio (Nasdaq: TBIO), a clinical-stage messenger RNA (mRNA) therapeutics company, today presented positive results from a preclinical study ...

“Patients with PCD have characteristic clinical features that distinguish [PCD] from other respiratory conditions of childhood, and diagnostic testing should be considered only in those who have a ...

Primary ciliary dyskinesia (PCD) is a congenital disorder of heterogeneous genetic origin. It is inherited in an autosomal recessive manner. It is a member of the ciliopathies, and has diverse ...