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1. 原発性線毛機能不全（線毛不動症候群） primary ciliary dyskinesia immotile cilia syndrome
2. 小児における気管支拡張症の原因 causes of bronchiectasis in children
3. 成人における気管支拡張症の臨床症状および診断 clinical manifestations and diagnosis of bronchiectasis in adults
4. 小児における慢性咳嗽に対するアプローチ approach to chronic cough in children
5. 小児における喘息以外の喘鳴疾患 wheezing illnesses other than asthma in children

English Journal

Diagnosis and management of primary ciliary dyskinesia.

Lucas JS1, Burgess A, Mitchison HM, Moya E, Williamson M, Hogg C; on behalf of the National PCD Service, UK.
Archives of disease in childhood.Arch Dis Child.2014 Apr 25. doi: 10.1136/archdischild-2013-304831. [Epub ahead of print]
Primary ciliary dyskinesia (PCD) is an inherited autosomal-recessive disorder of motile cilia characterised by chronic lung disease, rhinosinusitis, hearing impairment and subfertility. Nasal symptoms and respiratory distress usually start soon after birth, and by adulthood bronchiectasis is invaria
PMID 24771309

Primary ciliary dyskinesia diagnosed on nasal mucosal biopsy in two newborns.

Yasuhara J1, Yamada Y, Hara K, Suhara R, Hattori Y, Yamaguchi T, Mizuno Y, Kizu R, Bamba M.
Pediatrics international : official journal of the Japan Pediatric Society.Pediatr Int.2014 Apr;56(2):258-261. doi: 10.1111/ped.12268.
Primary ciliary dyskinesia (PCD) is a genetic disease that causes abnormalities in ciliary structure and/or function. Ciliated cells line the upper and lower respiratory tracts and the Eustachian tube. Impairment of mucus clearance at these sites leads to sinusitis, repeated pulmonary infections, br
PMID 24730627

Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype.

Knowles MR1, Ostrowski LE, Leigh MW, Sears PR, Davis SD, Wolf WE, Hazucha MJ, Carson JL, Olivier KN, Sagel SD, Rosenfeld M, Ferkol TW, Dell SD, Milla CE, Randell SH, Yin W, Sannuti A, Metjian HM, Noone PG, Noone PJ, Olson CA, Patrone MV, Dang H, Lee HS, Hurd TW, Gee HY, Otto EA, Halbritter J, Kohl S, Kircher M, Krischer J, Bamshad MJ, Nickerson DA, Hildebrandt F, Shendure J, Zariwala MA.
American journal of respiratory and critical care medicine.Am J Respir Crit Care Med.2014 Mar 15;189(6):707-17. doi: 10.1164/rccm.201311-2047OC.
RATIONALE: Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia, but the genetic cause is not defined for all patients with PCD.OBJECTIVES: To identify disease-causing mutations in novel genes, we performed exome sequencing, follow-up characterization, m
PMID 24568568

Japanese Journal

症例繰り返し結石を喀出したKartagener症候群の1例

鈴木和夫,梶原大季,笠井昭男 [他]
日本呼吸器学会誌 = Annals of the Japanese Respiratory Society 3(2), 293-296, 2014-03-10
NAID 40020030944

原発性線毛運動不全症―最近の進歩

竹内万彦
耳鼻咽喉科臨床 107(5), 345-353, 2014
… Cases with situs inversus are termed "Kartagener's syndrome" and usually these diagnoses are not difficult to make. …
NAID 130004553869

Kartagener's Syndrome and Rheumatoid Arthritis

Takasaki Satoshi,Yamakage Shu,Fukase Sachiko,Takahashi Toshiyuki
Internal Medicine 53(3), 269-274, 2014
… We herein present the case of a 47-year-old woman with rheumatoid arthritis (RA) complicated by Kartagener's syndrome (KS). …
NAID 130003392639

Related Pictures

Kartagener Syndrome; Ciliary Dyskinesia Kartagener syndrome | Radiology Case Kartagener's Syndrome | Flickr - Photo type kartagener; triade de kartagener Kartagener syndrome | Image | Radiopaedia