Primary ciliary dyskinesia

An autosomal recessive primary ciliary motility defect caused by mutation(s) in the CCDC40 gene, encoding coiled-coil domain-containing protein 40.

Disease Alternative Name

primary ciliary dyskinesia 15
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Recent Cases of Primary ciliary dyskinesia

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Concluded Case

Researchers reported a case of Situs Inversus Totalis that has appeared in the New England Journal of medicine. What is...See More

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Concluded answer

THE CONDITION IS ALSO ASSOCIATED WITH AGENESIS OF FRONTAL AND MAXILLARY SINUSES.


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