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Kartagener’s syndrome: A case report [PDF]

Vojnosanitetski Pregled, 2016
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 ...
Taušan Đorđe, Ristić Anđelka, Zvezdin Biljana   +2 more
doaj   +3 more sources

Takotsubo’s Cardiomyopathy in a Patient with Kartagener’s Syndrome [PDF]

Case Reports in Medicine, 2014
A 46-year-old African-American male with past medical history significant for Kartagener’s syndrome, essential hypertension, and HIV presented with acute chest pain. ECG and troponins indicated an acute myocardial infarction.
Luis W. Dominguez, Robert P. Doggette, Fernando Gonzalez-Ibarra, Imam H. Shaik, Amer K. Syed   +4 more
doaj   +2 more sources

Surgical Challenges in Papillary Thyroid Cancer Patient With Kartagener's Syndrome: A Case Report

Clinical Case Reports
Kartagener's syndrome is a rare disorder defined by situs inversus, chronic sinusitis, and bronchiectasis, with mirror‐image anatomy that may alter recurrent laryngeal nerve course and vascular structures.
Jianhao Huang, Tingting Zhao, Minghui Wei   +2 more
doaj   +2 more sources

Renal Carcinoma and Kartagener Syndrome: An Unusual Association

Case Reports in Urology, 2020
Background. The association of renal cell carcinoma and Kartagener’s syndrome is unusual, and only eleven cases have been reported in the literature. The purpose of this work is to analyze this unusual association of Kartagener’s syndrome and renal cell ...
Hamza Dergamoun, Abdelilah El Alaoui, Imad Boualaoui, Hachem Sayegh, Lounis Benslimane, Yassine Nouini   +5 more
doaj   +2 more sources

Surgical Management of Kartagener's Syndrome With Bronchiectasis in a Pediatric Patient: A Case Report on Right Lower Lung Lobectomy in a 9‐Year‐Old Female

Clinical Case Reports
Kartagner syndrome is a rare congenital autosomal recessive disorder of ciliary movement, characterized by triad of chronic sinusitis, situs inversus and bronchiectasis leading to recurrent chest and sinuses infections.
Pakeezah Tabasum, Makhdooom Bilawal, Priya Devi, Waseem Sajjad, Ali Raza Brohi, Mohammed Hammad Jaber Amin   +5 more
doaj   +2 more sources

Management of Primary Ciliary Dyskinesia in a Kartagener's Syndrome Patient With Total Situs Inversus

Respirology Case Reports
Kartagener's syndrome is a rare, autosomal recessive disorder characterised by primary ciliary dyskinesia (PCD) resulting in impaired mucociliary clearance and situs inversus.
Ivan H. Huang, Kenneth N. Dang, Saarang Kashyap, Alexander J. Sweidan   +3 more
doaj   +2 more sources

Rheumatoid Arthritis, Kartagener’s Syndrome, and Hyperprolactinemia: Who Started It? [PDF]

Case Reports in Rheumatology, 2016
We report a case of an 18-year-old girl who presented to our hospital with history of recurrent respiratory infections, amenorrhea, and symmetric polyarthritis.
Hussein Halabi, Israa Mulla
doaj   +2 more sources

Kartagener Syndrome: A Rare Cause of Infertility

Gynecology Obstetrics & Reproductive Medicine, 2015
Kartagener’s syndrome is defined as motility dysfunction of the epithelial cilia lining the respiratory tract, fallopian tubes and the flagella of the sperm and genetically classified as a rare autosomal recessive disease consisting almost half of all ...
Kadir Bakay, Davut Güven, İdris Koçak
doaj   +1 more source

Management of Prosthetic Mitral Valve Infective Endocarditis in a Patient With Congenital Heart Disease

JACC: Case Reports
We present the case of an adult patient with Kartagener’s syndrome, multiple prior sternotomies, and recurrent prosthetic valve endocarditis, a scenario without clear guidelines to direct management.
Nadir Emre Herdan, MD, Richard Ferraro, MD, Francoise Adeline Marvel, MD, Stephanie Leigh Alden, MD, Ari Michael Cedars, MD   +4 more
doaj   +2 more sources

Bone marrow involvement of a patient with Niemann-Pick disease concomitant with Kartagener’s syndrome: Report of a rare case

Mediterranean Journal of Hematology and Infectious Diseases, 2014
Niemann-Pick disease is a rare lipid storage disorder with autosomal recessive inheritance, which is characterized by accumulation of sphingomyelin and other sphingolipids in macrophages. In most cases, macrophage lipids show a non-spesific, ?ntense blue
Muzaffer Keklik, serdar sivgin, suleyman baldane, afra yildirim, olgun kontas, fatih kardas, cigdem pala, ali unal   +7 more
doaj   +1 more source