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.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117 Pediatr+Pulmonol
2016 ; 51
(2
): 115-32
Nephropedia Template TP
gab.com Text
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English Wikipedia
Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD
foundation consensus recommendations based on state of the art review
#MMPMID26418604
Shapiro AJ
; Zariwala MA
; Ferkol T
; Davis SD
; Sagel SD
; Dell SD
; Rosenfeld M
; Olivier KN
; Milla C
; Daniel SJ
; Kimple AJ
; Manion M
; Knowles MR
; Leigh MW
Pediatr Pulmonol
2016[Feb]; 51
(2
): 115-32
PMID26418604
show ga
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous, rare lung
disease resulting in chronic oto-sino-pulmonary disease in both children and
adults. Many physicians incorrectly diagnose PCD or eliminate PCD from their
differential diagnosis due to inexperience with diagnostic testing methods. Thus
far, all therapies used for PCD are unproven through large clinical trials. This
review article outlines consensus recommendations from PCD physicians in North
America who have been engaged in a PCD centered research consortium for the last
10 years. These recommendations have been adopted by the governing board of the
PCD Foundation to provide guidance for PCD clinical centers for diagnostic
testing, monitoring, and appropriate short and long-term therapeutics in PCD
patients.
|Biopsy
[MESH]
|Breath Tests
[MESH]
|Chronic Disease
[MESH]
|Disease Management
[MESH]
|Genetic Testing
[MESH]
|Humans
[MESH]
|Influenza Vaccines/therapeutic use
[MESH]
|Kartagener Syndrome/*diagnosis/*therapy
[MESH]
|Microscopy, Electron
[MESH]
|Microscopy, Video
[MESH]
|North America
[MESH]
|Pneumococcal Vaccines/therapeutic use
[MESH]
|Respiratory Syncytial Virus Vaccines/therapeutic use
[MESH]