Primary ciliary dyskinesia overview: Difference between revisions
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==Overview== | ==Overview== | ||
Primary ciliary dyskinesia is an [[autosomal recessive]] disorder characterised by functional defects in the [[cilia]] resulting in a abnormal mucociliary clearance. | |||
==Historical Perspective== | ==Historical Perspective== | ||
Revision as of 14:08, 28 July 2021
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Primary ciliary dyskinesia Microchapters |
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Differentiating Primary ciliary dyskinesia from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Primary ciliary dyskinesia overview On the Web |
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American Roentgen Ray Society Images of Primary ciliary dyskinesia overview |
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Risk calculators and risk factors for Primary ciliary dyskinesia overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Hafsa Ghaffar, M.B.B.S[2]
Overview
Primary ciliary dyskinesia is an autosomal recessive disorder characterised by functional defects in the cilia resulting in a abnormal mucociliary clearance.