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Kartagener Syndrome

More information in Books or onNLM PubMed
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.      Other names Kartagener Triad; Ciliary Dyskinesia, Primary; Triad, Kartagener's; Triad, Kartagener; Syndrome, Siewert; Syndrome, Kartagener's; Syndrome, Kartagener; Primary Ciliary Dyskinesia; Polynesian Bronchiectases; Kartageners Triad; Kartageners Syndrome; Dyskinesia, Primary Ciliary; Bronchiectasis, Polynesian; Siewert Syndrome; Polynesian Bronchiectasis; Kartagener's Triad; Kartagener's Syndrome; Dextrocardia, Bronchiectasis, and Sinusitis
 
SubstanceCAS Registry & nameCategoriesSource
Primary ciliary dyskinesia, 4  0   *Kartagener Syndrome.
Primary ciliary dyskinesia, 3  0   *Kartagener Syndrome.
Primary ciliary dyskinesia, 2  0   *Kartagener Syndrome.
DPCD protein, human  0   *Proteins Kartagener Syndrome. Am J Respir Cell Mol biol 2004 Apr;30(4):428-34

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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