Kartagener Syndrome [Kartagenerův syndrom]

topical
46
Terms

Kartagenerova triáda
Kartagenerova trias
polynézská bronchiektazie
polynézská bronchiektázie
primární ciliární dyskineze 1
Siewertův syndrom

 

Ciliary Dyskinesia, Primary, 1
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
Dextrocardia, Bronchiectasis, and Sinusitis
Kartagener Triad
Kartagener's Syndrome
Kartagener's Triad
Polynesian Bronchiectasis
Siewert Syndrome

Persistent link   https://www.medvik.cz/link/D007619
Definition

An autosomal recessive disorder characterized by a triad of DEXTROCARDIA; INFERTILITY; and SINUSITIS. The syndrome is caused by mutations of DYNEIN genes encoding motility proteins which are components of sperm tails, and CILIA in the respiratory and the reproductive tracts.

DUI
D007619 MeSH Browser
CUI
M0011929
History note
2002 (1963); for CILIARY DYSKINESIA, PRIMARY use CILIARY MOTILITY DISORDERS 1992-2001
Public note
2002; see KARTAGENER'S SYNDROME 1990-2001; see KARTAGENER TRIAD 1963-1989; for CILIARY DYSKINESIA, PRIMARY see CILIARY MOTILITY DISORDERS 1992-2001

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications 2
DI
diagnosis 19
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology 2
EH
ethnology
ET
etiology 9
GE
genetics 9
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 1
PP
physiopathology 3
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation 2
SU
surgery
TH
therapy 8
UR
urine
VE
veterinary
VI
virology

C Diseases
C08 Respiratory Tract Diseases 2 218
C08.127 Bronchial Diseases 352
C08.127.384 Bronchiectasis 144
C08.127.384.500 Kartagener Syndrome 46
C08.200 Ciliary Motility Disorders 57
C08.200.531 Kartagener Syndrome 46
C08.695 Respiratory System Abnormalities 39
C08.695.195 Bronchogenic Cyst 18
C08.695.214 Bronchopulmonary Sequestration 17
C08.695.271 Choanal Atresia 15
C08.695.290 Cystic Adenomatoid Malformation of Lung, Congenital 9
C08.695.501 Kartagener Syndrome 46
C08.695.520 Laryngocele 6
C08.695.815 Scimitar Syndrome 3
C08.695.830 Tracheobronchomegaly 2
C09 Otorhinolaryngologic Diseases 678
C09.150 Ciliary Motility Disorders 57
C09.150.531 Kartagener Syndrome 46
C14 Cardiovascular Diseases 10 507
C14.240 Cardiovascular Abnormalities 91
C14.240.400 Heart Defects, Congenital 1 559
C14.240.400.280 Dextrocardia 21
C14.240.400.280.500 Kartagener Syndrome 46
C14.280 Heart Diseases 2 867
C14.280.400 Heart Defects, Congenital 1 559
C14.280.400.280 Dextrocardia 21
C14.280.400.280.500 Kartagener Syndrome 46
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 741
C16.131.077 Abnormalities, Multiple 330
C16.131.077.245 Ciliopathies 9
C16.131.077.245.500 Ciliary Motility Disorders 57
C16.131.077.245.500.531 Kartagener Syndrome 46
C16.131.240 Cardiovascular Abnormalities 91
C16.131.240.400 Heart Defects, Congenital 1 559
C16.131.240.400.280 Dextrocardia 21
C16.131.240.400.280.500 Kartagener Syndrome 46
C16.131.740 Respiratory System Abnormalities 39
C16.131.740.195 Bronchogenic Cyst 18
C16.131.740.214 Bronchopulmonary Sequestration 17
C16.131.740.271 Choanal Atresia 15
C16.131.740.290 Cystic Adenomatoid Malformation of Lung, Congenital 9
C16.131.740.501 Kartagener Syndrome 46
C16.131.740.650 Laryngocele 6
C16.131.740.658 Laryngostenosis 33
C16.131.740.815 Scimitar Syndrome 3
C16.131.740.830 Tracheobronchomegaly 2
C16.131.810 Situs Inversus 33
C16.131.810.250 Dextrocardia 21
C16.131.810.250.500 Kartagener Syndrome 46
C16.320 Genetic Diseases, Inborn 1 213
C16.320.033 Adrenal Hyperplasia, Congenital 225
C16.320.051 Alagille Syndrome 19
C16.320.060 alpha 1-Antitrypsin Deficiency 83
C16.320.070 Anemia, Hemolytic, Congenital 48
C16.320.077 Anemia, Hypoplastic, Congenital 3
C16.320.080 Ataxia Telangiectasia 47
C16.320.089 Autoimmune Lymphoproliferative Syndrome 2
C16.320.099 Blood Coagulation Disorders, Inherited 61
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.144 Camurati-Engelmann Syndrome 6
C16.320.160 Cardiomyopathy, Hypertrophic, Familial 32
C16.320.165 CHARGE Syndrome 1
C16.320.170 Cherubism 1
C16.320.180 Chromosome Disorders 259
C16.320.184 Ciliopathies 9
C16.320.184.500 Ciliary Motility Disorders 57
C16.320.184.500.531 Kartagener Syndrome 46
C16.320.188 Costello Syndrome 3
C16.320.190 Cystic Fibrosis 1 328
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 97
C16.320.290 Eye Diseases, Hereditary 57
C16.320.298 Familial Multiple Lipomatosis
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 1
C16.320.322 Genetic Diseases, X-Linked 59
C16.320.338 Genetic Diseases, Y-Linked 1
C16.320.355 Hajdu-Cheney Syndrome 6
C16.320.365 Hemoglobinopathies 68
C16.320.382 Hereditary Autoinflammatory Diseases 46
C16.320.400 Heredodegenerative Disorders, Nervous System 45
C16.320.413 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.427 Hyperthyroxinemia, Familial Dysalbuminemic 1
C16.320.447 Imprinting Disorders
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.495 Lennox Gastaut Syndrome 5
C16.320.510 Loeys-Dietz Syndrome 7
C16.320.540 Marfan Syndrome 105
C16.320.565 Metabolism, Inborn Errors 711
C16.320.577 Muscular Dystrophies 140
C16.320.590 Myasthenic Syndromes, Congenital 20
C16.320.600 Nail-Patella Syndrome 8
C16.320.700 Neoplastic Syndromes, Hereditary 143
C16.320.709 Oculocerebrorenal Syndrome 9
C16.320.714 Orofaciodigital Syndromes 7
C16.320.718 Osteoarthropathy, Primary Hypertrophic 127
C16.320.728 Osteochondrodysplasias 123
C16.320.737 Osteogenesis Imperfecta 106
C16.320.775 Pain Insensitivity, Congenital 10
C16.320.784 Pelger-Huet Anomaly 7
C16.320.798 Primary Immunodeficiency Diseases 46
C16.320.812 Pycnodysostosis 2
C16.320.831 Renal Tubular Transport, Inborn Errors 36
C16.320.850 Skin Diseases, Genetic 89
C16.320.925 Werner Syndrome 14
C16.320.962 Yellow Nail Syndrome

Ciliary Dyskinesia, Primary, 7 Disease MeSH Browser

Ciliary Dyskinesia, Primary, 8 Disease MeSH Browser

Ciliary Dyskinesia, Primary, 9 Disease MeSH Browser

Primary ciliary dyskinesia, 2 Disease MeSH Browser

Primary ciliary dyskinesia, 3 Disease MeSH Browser

Primary ciliary dyskinesia, 4 Disease MeSH Browser

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