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Kartegnar syndrome

Kartagener syndrome: A case report - PubMed Central (PMC

  1. Kartagener syndrome is a rare, autosomal recessive genetic disorder that causes defects in the action of ciliary movement, comprises of triad situs inversus, chronic sinusitis, and bronchiectasis. We present the case of a 3-year-old boy with repeated respiratory infections and pneumonic infections presenting with acute respiratory failure
  2. Background: Kartagener's syndrome is a subset of primary ciliary dyskinesia, an autosomal recessive inherited disorder characterized by the clinical triad of chronic sinusitis, bronchiectasis, and situs inversus. Abnormal ciliary structure or function leading to impaired ciliary motility is the main pathophysiologic problem in Kartagener's syndrome
  3. Kartagener syndrome (also known as Kartagener-Afzelius syndrome) is a subset of primary ciliary dyskinesia, an autosomal recessive condition characterized by abnormal ciliary structure or function, leading to impaired mucociliary clearance
  4. al situs inversus as well as the presence of immotile cilia that predispose to sinusitis, otitis media, and bronchiectasis. The ciliary immotility is due to a deficiency of the dynein arms of the cilia

Kartagener's Syndrome (KS), also known as ciliary dyskinesia syndrome or primary ciliary dyskinesia (PCD), is a rare genetic disease in which some cellular elements (cilia and flagella) do not function properly. This genetic disorder causes alterations in ciliary motility due to mutations in different genes Kartagener syndrome is a very rare hereditary disorder that is caused by defects in the genes. It is autosomal recessive, meaning that it only occurs if both parents carry the gene. Kartagener syndrome affects approximately 30,000 people, including all genders Kartagener's syndrome is a rare genetic disorder. It involves abnormalities of your cilia, which can cause a variety of health problems. It also involves situs inversus, a condition in which your..

متلازمة كارتاجنر هي مرض وراثي نادر، تسببه طفرة تصيب جينات مختلفة. لكن توريث الطفرة جسدي متنحٍ، أي أنك يجب أن ترث الجين المصاب من كلا والديك حتى تصاب بالمرض Kartagener Syndrome is genetic, congenital disorder, which affects lungs and also male reproductive organs. In this disease, the cilia, which assisting in transporting mucus in the respiratory tract get affected and may mucous unable to move or move incorrectly Kartagener syndrome is also known as ciliary dyskinesia syndrome or primary ciliary dyskinesia (PCD). It is a rare genetic disease which affect lungs and also reproductive organs. It is caused by a mutation that can occur on different genes

متلازمة كارتاجنر (بالإنجليزية: Kartagener syndrome)‏ هي أحد أنواع خلل الحركة الهدبي الأولي. عندما يكون خلل الحركة الهدبي الأولي ترافقه أعراض التهاب الجيوب المزمن وأحشاء مقلوبة الموضع وتوسع القصبات فإنه يدعى بمتلازمة كارتاجنر What is Kartagener syndrome. Kartagener syndrome is a type of primary ciliary dyskinesia that is characterized by triad of chronic sinusitis, bronchiectasis, and situs inversus totalis (mirror-image reversal of internal organs) 1).Kartagener syndrome signs and symptoms vary but may include neonatal respiratory distress; frequent lung, sinus and middle ear infections beginning in early. Kartagener Syndrome, also known as Primary Ciliary Dyskinesia (PCD), is an autosomal recessive disorder caused by a dynein arm defect affecting the movement of cilia. Ciliary immotility leads to the classic Kartagener Syndrome triad of findings: chronic sinusitis, bronchiectasis, and situs inversus. Immotile cilia cause sinusitis and upper respiratory infections (otitis media) by impairing.

Kartagener Syndrome, also known as Primary Ciliary Dyskinesia (PCD), is an autosomal recessive disorder that is characterized by a dynein arm defect. This ca.. Animated Mnemonics (Picmonic): https://www.picmonic.com/viphookup/medicosis/ - With Picmonic, get your life back by studying less and remembering more. M..

Kartagener syndrome is one of the ciliary dyskinesia (or immotile cilia) syndromes. The presenting symptoms are a constellation of recurrent pulmonary infections, chronic sinusitis, recurrent otitis media, situs inversus, and infertility (in males). Structural ciliary abnormalities (most common are absent dynein arms) result in abnormal ciliary. • Kartagener's Syndrome should always be considered in patients with recurrent respiratory infections and hx of situs inversus • Symptoms result from impaired mucociliary clearance • Clinical features include: • recurrent respiratory infections • bronchiectasis • sinusitis • chronic otitis • dextrocardia - situs inversu When accompanied by the combination of situs inversus (reversal of the internal organs), chronic sinusitis, and bronchiectasis, it is known as Kartagener syndrome (only 50% of primary ciliary dyskinesia cases include situs inversus). [citation needed] Treatment. There are no standardized effective treatment strategies for the condition Kartagener's syndrome is a rare, autosomal recessive inherited disease, which is characterized by a triad of chronic sinusitis, bronchiectasis, and situs inversus. In this report, we aimed to represent the effect of aerobic exercise training in addition to chest physiotherapy in an outpatient with Kartagener's syndrome

Kartagener's syndrome: a case repor

  1. When situs inversus, chronic sinusitis, and bronchiectasis occur together, an individual is said to have Kartagener syndrome. The genetics, clinical manifestations, diagnosis, and management of PCD are reviewed here. The evaluation and treatment of bronchiectasis are discussed separately
  2. The Kartagener syndrome is an autosomal recessive condition characterized by primary ciliary dyskinesia, abnormal frontal sinuses and situs inversus. Kartagener Syndrome (PCD): Read more about Symptoms, Diagnosis, Treatment, Complications, Causes and Prognosis
  3. Case Discussion. Kartagener syndrome, first described in 1933, is characterized by the triad of situs inversus, bronchiectasis and sinusitis and/or nasal polyposis. It is present in 50% of patients with primary ciliary dyskinesia, a rare genetic disorder causing ciliary defects and impaired mucociliary clearance, thereby predisposing patients to otosinopulmonary disease
  4. Kartagener syndrome: ( kahr-tag'ĕ-nĕr ), [MIM*244400] complete situs inversus associated with bronchiectasis and chronic sinusitis associated with ciliary dysmotility and impaired ciliary mucous transport in the respiratory epithelium. The mechanism of the reversal of laterality remains an enigma, but it appears to be strictly an abolition.
  5. derde beweeglijkheid van de trilharen (cilia). Doordat hierdoor de luchtwegen worden aangetast, ontstaan er blijvende verwijdingen van de luchtwegen (bronchiën), aangeduid als bronchiëctasie en een chronische bijholteontsteking

Kartagener syndrome is sometimes known as the Siewert syndrome (Siewert, 1904). Eliasson et al. (1977) is credited with the term 'immotile cilia syndrome' (Afzelius, 2004). In vitro studies have shown that various patterns of abnormal ciliary beating (Rossman et al., 1980; Rutland and Cole, 1980) are the most frequently observed abnormalities. Das Kartagener-Syndrom, auch Kartagener-Trias genannt, ist ein angeborenes Syndrom mit seitenverkehrter Anlage der inneren Organe (Situs inversus), Bronchiektasen und Unterentwicklung oder Nichtausbildung der Nasennebenhöhlen und Warzenfortsatzzellen sowie Nasenpolypen, einhergehend mit chronischer polypöser Nasennebenhöhlen-Entzündung ().Die Bewegung des Flimmerepithels (der Cilien) in. Abstract. Kartagener syndrome (KS), an autosomal recessively inherited disease, is characterized by the triad of situs inversus, bronchiectasis and sinusitis. This disorder affects the activity of proteins important to the movement of cilia, especially in the respiratory tract and the spermatozoa, developing a series of systemic alterations.

متلازمة كارتجنر (بالإنجليزية: Kartagener's Syndrome) أو ما يعرف بالقلب اليمين، هي عبارة عن مجموعة من الأعراض التي تشمل وجود القلب في الجهة اليمنى من الجسم، وتوسع القصبات الهوائية، والتهاب الجيوب الأنفية Kartagener's Syndrome. Kartagener's Syndrome is a hereditary genetic disease, described in 1933, it shows a low incidence in the population (1: 20,000 cases approx.) and occurs from birth. Its inheritance is autosomal recessive, which means that both members of the couple are carriers of the disease Description. Kartagener syndrome (KS) is an inherited disorder (autosomal recessive ) characterised by the clinical triad of chronic sinusitis; bronchiectasis; and situs inversus. It is is a subset of primary ciliary dyskinesia with abnormal ciliary structure/function associated with impaired ciliary motility Kartagener's syndrome is a rare disorder with constellation of bronchiectasis, infertility, siyus inversus and sinusitis. The aim of this article was to present classic findings of Kartagener's syndrome, so that patients with recurrent sinusitis and cough with sputum can be evaluated for primary ciliary dyskinesia. 5 Kartagener syndrome is part of the larger group of disorders referred to as primary ciliary dyskinesias. Approximately one half of patients with primary ciliary dyskinesia have situs inversus and, thus, are classified as having Kartagener syndrome. Afzelius proposed that normal ciliary beating is necessary for visceral rotation during embryonic.

Kartagener syndrome Radiology Reference Article

Synonyms: Dextrocardia bronchiectasis and sinusitis, Siewert syndrome, Immotile cilia syndrome, Kartagener type, Primary ciliary dyskinesia, Kartagener type, Dextrocardia-bronchiectasis-sinusitis syndrome, Primary ciliary dyskinesia and situs inversu Medical definition of Kartagener's syndrome: an abnormal condition inherited as an autosomal recessive trait and characterized by situs inversus, abnormalities in the protein structure of cilia, and chronic bronchiectasis and sinusitis Kartagener syndrome is a rare, ciliopathic, autosomal recessive genetic disorder that causes a defect in the action of the cilia lining the respiratory tract and fallopian tube Kartagener syndrome is a rare, autosomal recessive genetic disorder that causes defects in the action of ciliary movement, comprises of triad situs inversus, chronic sinusitis, and bronchiectasis. We present the case of a 3-year-old boy with repeated respiratory infections and pneumonic infection

Kartagener Syndrome is a condition that means the combination of bronchiectasis, recurrent sinusitis and situs inversus, which means that the organ +90 507 430 15 56; English Mirror-image reversal of organs : Kartagener Syndrome. This is a kind of Primary Ciliary Dyskinesia, where in the affected has mirrored position of his organs. Primary Ciliary Dyskinesia is a condition where the cilia and flagella of the cells fail to move. Cilia are fine, microscopic projections found on the surface of the cells of the. Kartagener's Syndrome List of authors. Kenneth Zurcher, M.D., and Akira Kawashima, M.D., Ph.D. A 46-year-old woman presented with cough, shortness of breath, and fevers. Imaging showed.

Kartagener's syndrome (KS) is a hereditary disease with typical symptoms of situs inversus, bronchiectasis, and chronic infections of the nasal mucosa. Autosomal recessive inheritance cannot be doubted on account of repeated observations of affected sibs and parental cansanguinity. The bronchopulmonary symptoms in sibs, however, cannot be explained by this mode of inheritance Kartagener syndrome is an autosomal recessive disor der with a triad of bronchiectasis, recurrent episodes of sinusitis and situs inversus in early life, with reduced fertility in the later part. Das Kartagener-Syndrom ist eine äußerst selten vorkommende Erbkrankheit.In Deutschland sind etwa 4000 Menschne von ihr betroffen. Bei circa 900 Patienten handelt es sich um Kinder oder Jugendliche. Das Syndrom ist eng mit der primären ciliären Dyskenesie (PCD) verbunden, die eine genetische Störung der beweglichen Zilien (Flimmerhärchen) darstellt

Kartagener Syndrome - an overview ScienceDirect Topic

Based on the clinical presentation and radiological findings, Kartagener syndrome (KS) was diagnosed. Empirical antibiotic therapy and supportive pulmonary care were initiated, and the patient was discharged with the resolution of symptoms 1 week later Kartagener syndrome is a rare, autosomal recessive congenital disease characterized by bronchiectasis, chronic pansinusitis and situs inversus, and is part of a broad group of conditions caused by primary ciliary dyskinesia [18,26]. Primary ciliary dyskinesia, previously known as immotile-cilia syndrome [1,29], is caused by ultrastructural.

Kartagener Syndrome: Definition, Causes and Symptom

Abstract: Kartagener syndrome is a rare, ciliopathic, autosomal recessive genetic disorder that causes a defect in the action of the cilia lining the respiratory tract and fallopian tube. Patients usually present with chronic recurrent rhinosinusitis, otitis media, pneumonia, and bronchiectasis caused by pseudomonal infection Primary ciliary dyskinesia is a disorder characterized by chronic respiratory tract infections, abnormally positioned internal organs, and the inability to have children (infertility). The signs and symptoms of this condition are caused by abnormal cilia and flagella. Explore symptoms, inheritance, genetics of this condition Kartagener syndrome is a subset of primary ciliary dyskinesia, an autosomal recessive condition characterized by abnormal ciliary structure and/or function, leading to impaired mucociliary clearance. Epidemiology The prevalence of primary ciliary dyskinesia is approximately 1 in 12,000-60,000 year-old child with Kartagener's syndrome. Paediatr Anaesth. 2003;13(8):714-7 12. Gávai M, Hupuczi P, Berkes E, Beke A, Hruby E, Murber A, Urbancsek J, Papp Z. Spinal anesthesia for cesarean section in a woman with Kartagener's syndrome and a twi Kartagener Syndrome (KS) is a rare autosomal recessive genetic disorder, resulting in a group of clinical manifestations, including bronchiectasis, chronic pansinusitis and situs inversus. We hereby reviewed eight cases of this rare entity selected from patients attending our outpatients Respiratory Unit since 2006. Samples of respiratory epithelium were obtained with the method of nasal.

Kartagener Syndrome Symptoms and Treatmen

  1. Kartagener's syndrome is a recessive autosomal disease which is mainly seen to affect ciliary movement 1. The incidence of Kartagener's syndrome is 1-2/30,000 births. Siewert first de-scribed the combination of situs inversuschronic sinusitis, and bronchiectasis in 1904 2. Manes Kartagener, a pulmonologist i
  2. Kartagener Syndrome. 508 likes · 87 talking about this. I'm not a doctor or a health coach; I'm a girl living with this illness! I share my story to inspire you and push you to do better! You're not..
  3. Kartagener's syndrome is a variant of the immotile cilia syndrome. 2 This has also been called primary ciliary dyskinesia and is a result of an autosomal recessive disorder of the microtubules of ciliated cells. Symptoms include male sterility, chronic or recurrent respiratory tract infection, and bronchiectasis because of the absence of.
  4. IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading.NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a.
  5. Description et symptômes du Syndrome de Kartagener (dyskinésie ciliaire primitive -DCP-). Ce syndrome est également connu comme le syndrome de dyskinésie ciliaire primitive (DCP). Il se caractérise par des altérations dans la structure et la fonction des cils présents dans les cellules du système respiratoire et des tissus gonadiques (Trompes de Fallope et spermatozoïdes)
  6. Skeik N, Jabr Fl. Kartagener syndrome. Int J Gen Med. Jan/2011. 12:41-43. . Marthin JK, Petersen N, Skovgaard LT, Nielsen KG. Lung function in patients with primary ciliary dyskinesia: a cross.
  7. Kartagener Syndrome is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings).Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity

El síndrome de Kartagener (SK) 1 es una variante clínica de la discinesia ciliar primaria caracterizado por la tríada situs inversus (corazón a la derecha, dextrocardia), bronquiectasias (dilatación patológica de los bronquios originado por infecciones crónicas de las vías respiratorias) y sinusitis (inflamación de uno o más senos paranasales); el situs inversus puede ser parcial. Kartagener syndrome is a clinical variation of primary ciliary dyskinesia, characterized by the classic triad of chronic sinusitis, bronchiectasis and situs inversus (total or partial), classified as a rare autosomal recessive inheritance disease Список тез доповідей конференцій на тему Kartagener syndrome. Наукові публікації для бібліографії з повним текстом pdf. Добірки джерел і теми досліджень Patients with Kartagener syndrome have a greater incidence of congenital cardiovascular defects, and recent studies have found that approximately 6% of patients with PCD have heterotaxy (situs.

Kartagener's syndrome (KS) is a rare autosomal recessive genetic disorder with a prevalence of 1:32,000, constituting about 50% of the primary ciliary dyskinesias (PCD) and characterized with a course including the triad of sinusitis, bronchiectasis and situs inversus. It was first described by Siewert in 1904, but Kartagener recognized in. T1 - Dysmotile cilia syndrome (Kartagener's) AU - Hartman, Thomas. PY - 2011/1/1. Y1 - 2011/1/1. N2 - Imaging description Dysmotile cilia syndrome or primary ciliary dyskinesia (PCD) leads to abnormalities in mucociliary clearance that can result in pulmonary and sinus disease

Kartagener syndrome is a type of p rimary ciliary dyskinesia that is also characterized by situs inversus totalis (mirror-image reversal of internal organs). The signs and symptoms vary but may include neonatal respiratory distress; frequent lung, sinus and middle ear infections beginning in early childhood; and infertility Kartagener Syndrome is a condition that means the combination of bronchiectasis, recurrent sinusitis and situs inversus, which means tha

Kartagener Syndrome Definition and Patient Educatio

  1. Kartagener's syndrome (final) 1. Kartagener's Syndrome<br />By: Jennifer Couture<br /> 2. Kartagener's syndrome known as Primary Cilia Dyskinesia. (1)<br />Rare genetic lung disorder (1)<br />Defect in action of the cilia lining the respiratory tract
  2. Kartagener's syndrome can affect Figure 1. Ectopic pregnancies (EP) and deliveries in 1983 and fertility to various degrees, and these women should be 1984 in Turku University Central Hospital, Finland. counselled accordingly, but should be encouraged by the possibility of conceiving and an ordinary course of gestation..
  3. Kartagener syndrome associated with mesangioproliferative glomerulonephritis Sriram Krishnamurthy, Bharat Choudhary, Nachiappa Ganesh Rajesh, Ananthakrishnan Ramesh, Sadagopan Srinivasan Department of Paediatrics, Jawaharlal Institute of Postgraduate Medical Education & Research (JIPMER), Pondicherry, India An 11-year-old girl with clinical features of Kartagener syndrome presented with signs.
  4. Most men with Kartagener's Syndrome have problems with the mobility of their sperm, as their tail or flagellum is altered. For this reason, the encounter between the sperm and the egg does not take place. This sperm alteration is known as asthenozoospermia. However, the spermatozoa are usually alive but lack mobility
  5. a relentless triad Betsy Ott 1933 Dr. Kartagener 4 cases Quantified the clinical triad: Bronchiectasis Chronic sinusitis Situs inversus Primary ciliary dyskinesia - A free PowerPoint PPT presentation (displayed as a Flash slide show) on PowerShow.com - id: 3b6ed8-MDU3

متلازمة كارتاجنر Kartagener Syndrome - أنا أصدق العل

Zur Unterstützung unserer Arbeit für Menschen mit dem Kartagener Syndrom und der Primären Ciliären Dyskinesie benötigen wir Ihre Hilfe. Online Spende. Veranstaltungen. 26 Sep 2021 05:00PM - 07:00PM Zoom-Loung Kinder, Jugendliche, Eltern: 30 Sep 2021 03:00PM - 05:00PM Zoom-Sitzung med. Beirat Le syndrome de Kartagener, maladie génétique très rare à transmission autosomique récessive, se caractérise par une triade : une bronchorrhée chronique avec bronchectasie, une sinusite chronique et un situs inversus. Ce syndrome fait partie d'un syndrome d'immobilité ciliaire primitive appelé la dyskinésie ciliaire primitive Kartagener's syndrome, an inherited immolile cilia syndrome, may present as recurrent orbital cellulitis and is a consideration in the differential diagnosis of orbital cellulitis occurring m young children. AB - Purpose. To present a case of Kartagener's -syndrome which presented as recurrent proptosis. Methods Search for: Rare Disease Profiles; 5 Facts; Rare IQ; Rare Mystery;

Kartagener Syndrome - Symptoms, Treatment, Diagnosis

Kartagener Syndrome - BioPharma Note

Kartagener's syndrome is characterized by mucociliary dysfunction of the respiratory tract and has a triad of features, including situs inversus totalis, chronic sinusitis [ncbi.nlm.nih.gov] Levocardia. Dextrocardia is a feature of Kartagener's syndrome Kartagener's syndrome is a subset of primary ciliary dyskinesia, an autosomal recessive inherited disorder characterized by the clinical triad of chronic sinusitis, bronchiectasis, and situs inversus. Abnormal ciliary structure or function leading to impaired ciliary motility is the main pathophysiologic problem in Kartagener's syndrome. A 24-year-old man from Gondar town, North-West. Kartagener's syndrome 2 (KS), which is currently classified as a subgroup of PCD, is characterized by the triad of bronchiectasis, paranasal sinusitis and SIT. We present a review of 14 patients with SIT, 11 of whom had KS. In 6 of these patients, there were signs of diffuse bronchiolitis (DB) on thoracic CT

متلازمة كارتاجنر - ويكيبيدي

Kartagener syndrome is a rare, ciliopathic, autosomal recessive genetic disorder that causes a defect in the action of the cilia lining the respiratory tract and fallopian tube. Patients usually present with chronic recurrent rhinosinusitis, otitis media, pneumonia, and bronchiectasis caused by pseudomonal infection Kartagener syndrome (KS). Inversion of situs in PCD is a random event as proved with monozygotic twins with discordant heart orientation [2]. Cilia rotation induces a leftward flow to the extraembryonic fluid. This flow may concentrate on the left side, or deplete on the right side, the critical factors that start the molecular cascad

Kartagener syndrome causes, symptoms, diagnosis & treatmen

[Kartagener syndrome; surgical treatment; lobectomy and segmentectomy; preliminary report]. TAIANA JA, VILLEGAS AH, SCHIEPPATI E. Rev Asoc Med Argent, 68(787-788):565-568, 01 Dec 1954 Cited by: 0 articles | PMID: 1438513 Kartagener syndrome (KS) is a rare autosomal recessive disorder related to defective function and structure of ciliated cells. The disorder affects the function of cilia lining the respiratory tract, fallopian tubes, and spermatozoa as well as the ciliary control of organ positioning during the embryogenic stage

Kartagener Syndrome Triad Usmle Step 1 Mnemoni

Kartagener: ( kahr-tag'ĕ-nĕr ), Manes, Swiss physician, 1897-1975. See: Kartagener syndrome , Kartagener triad Introduction. Kartagener syndrome (KS) is a rare autosomal recessive disorder with an incidence of 1 per 20,000-30,000 live births ().KS is a primary ciliary dyskinesia (PCD) characterized by situs inversus, paranasal sinusitis and bronchiectasis ().Clinical manifestations of KS usually present during childhood and include chronic rhinitis due to pansinusitis, cough, wheeze and shortness of. Learn Kartagener Syndrome (Primary Ciliary Dyskinesia) - Other Genetic Disorders for Medicine faster and easier with Picmonic's unforgettable videos, stories, and quizzes! Picmonic is research proven to increase your memory retention and test scores. Start learning today for free

Kartagener Syndrome Mnemonic for USMLE - YouTub

A-Z of Chest Radiology - July 2007. We use cookies to distinguish you from other users and to provide you with a better experience on our websites Evidence-based information on kartagener syndrome from hundreds of trustworthy sources for health and social care. Search results. Jump to search results. Filter Toggle filter panel Evidence type Add filter for Guidance and Policy (7) Add. Manes Kartagener (1897 - 1975) was an Austrian-Swiss physician.. He was the first to report the triad of situs inversus, chronic sinusitis and bronchiectasis in 1933, which is now eponymous with his name - Kartagener syndrome.The triad only represents half the cases of what is now known as primary ciliary dyskinesia (immotile cilia syndrome) Kartagener syndrome pronunciation with meanings, synonyms, antonyms, translations, sentences and more Which is the right way to pronounce the word Reciprocity? rec-i-proc-i-t Kartagener's syndrome is a condition defined by the symptomatic triad of situs inversus, sinusitis and bronchiectasis. Patients with PCD can also have abnormal orientation of some organs but not others, a condition called situs ambiguus or heterotaxy (Kennedy et al. 2007. PubMed ID: 17515466). Heterotaxy syndrome results from a failure to.

Kartagener's Syndrome (Immotile Cilia Syndrome or Primary

Kartagener syndrome could therefore be regarded as a subgroup of the immotile cilia syndrome. The clinical consequences are the same and include chronic cough and expectoration of mucoid, mucopurulent sputum, bronchiectasis, chronic rhinitis and nasal polyposis, recurrent maxillary rhinitis, often agenesis of the frontal sinuses, not rarely. Como é feito o tratamento. O tratamento da Síndrome de Kartagener tem como objetivo diminuir os sintomas e evitar o surgimentos de infecções respiratórias, sendo normalmente indicado tomar antibióticos para tratar sinusites, bronquites e pneumonia de acordo com a orientação médica. É também recomendado também o uso de soro fisiológico, mucolíticos ou broncodilatadores para. Kartagener syndrome 46 Kaufman-McKusick syndrome 47 Klippel-Feil syndrome 48 Klippel-Trénaunay-Weber syndrome (angioosteohypertrophy) 49 Larsen syndrome 50 Laurence-Moon syndrome 51 Lenz microphthalmos syndrome 52 Marfan syndrome 53 McCune-Albright syndrome 54 Meckel Gruber syndrome 55. The Kartagener Syndrome is a rare recessive autossomical disease including the triad: chronical sinusitis, bronchiectasis and situs inversus with dextrocardia. The incidence of this genetical disorder is estimated about 1/25,000. Our purpose in this case report is to include new informations for who search about this syndrome Kartagener syndrome consists of congenital bronchiectasis, sinusitis, and total situs inversus in half of the patients. A patient diagnosed with Kartagener syndrome was reffered to our department due to 3-vessel coronary disease. An off-pump coronary artery bypass operation was performed using both internal thoracic arteries and a saphenous vein graft