Primary ciliary dyskinesia causes: Difference between revisions
(Created page with "__NOTOC__ {{Primary ciliary dyskinesia}} {{CMG}} ==Overview== ==Causes== This disease in genetically inherited. Both inner and/or outer dynein arms are dysfunction and ...") |
m (Changes made per Mahshid's request) |
||
| Line 13: | Line 13: | ||
[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Pulmonology]] | [[Category:Pulmonology]] | ||
[[Category:Cardiology]] | [[Category:Cardiology]] | ||
[[Category:Disease]] | [[Category:Disease]] | ||
Revision as of 18:47, 18 September 2017
|
Primary ciliary dyskinesia Microchapters |
|
Differentiating Primary ciliary dyskinesia from other Diseases |
|---|
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
Primary ciliary dyskinesia causes On the Web |
|
American Roentgen Ray Society Images of Primary ciliary dyskinesia causes |
|
Risk calculators and risk factors for Primary ciliary dyskinesia causes |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Causes
This disease in genetically inherited. Both inner and/or outer dynein arms are dysfunction and thus the axoneme structure lacks the ability to move. Axonemes are the elongated structures that make up cilia and flagella. The dysfunction of the cilia begins during the embryologic phase of development. Since the cilia aid in the movement of growth factors resulting in the normal rotation of the internal organs during early embryological development, 50% of these individuals will develop situs inversus, as the laterality of the internal organs is determined by chance.