Kartagener’s syndrome: A case report
Introduction. Kartagener’s syndrome is a recessive autosomal disease which is mainly seen to affect ciliary movement. The symptoms of the syndrome are the consequence of the defective motility of the cilia found in the respiratory tract and that results with recurrent lung infections caused by mucus...
Saved in:
| Main Authors: | Taušan Đorđe, Ristić Anđelka, Zvezdin Biljana |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Ministry of Defence of the Republic of Serbia, University of Defence, Belgrade
2016-01-01
|
| Series: | Vojnosanitetski Pregled |
| Subjects: | |
| Online Access: | http://www.doiserbia.nb.rs/img/doi/0042-8450/2016/0042-84501600072T.pdf |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Kartagener’s Syndrome with Short Stature – A Rare Association
by: Thoyaj KJ, et al.
Published: (2025-04-01) -
Nasopharyngeal carcinoma in a child with Kartagener`s syndrome
by: Buket Kara, et al.
Published: (2021-02-01) -
EARLY DIAGNOSIS AND TREATMENT IN PATIENT WITH A PRIMARY CILIARY DYSKINESIA (KARTAGENER SYNDROME): CASE REPORT
by: I. V. Rybakova, et al.
Published: (2018-08-01) -
Kartagener syndrome with minimal change disease: a case report
by: Qun Huang, et al.
Published: (2025-04-01) -
Bone marrow involvement of a patient with Niemann-Pick disease concomitant with Kartagener’s syndrome: Report of a rare case
by: Muzaffer Keklik, et al.
Published: (2014-08-01)