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Kartagener Syndrome |11044|
Kartagener Syndrome Subsets
Immotile Cilia Syndrome, Kartagener Type
See Also ↔
 
 
“Kartagener Syndrome”  
  In our body, the inborn genetic dis-order, Kartagener Syndrome is an autosomal recessive health challenge, indicative to a specific set of signs, symptoms or other health indicators, characterized by the triad of dextrocardia, infertility, and sinusitis, caused by mutations of DYNEIN genes encoding motility proteins which are components of sperm tails, and cilia (ciliary motility dis-order) in the respiratory (respiratory system abnormality) and the reproductive tracts. *
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References & Citations:
1. Shiraishi K. et al "Young's syndrome associated with situs inversus totalis"   Arch Androl. 2004 May-Jun;50(3):169-72  
2. Merveille AC. et al "CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs"   Nat Genet. 2011 Jan;43(1):72-8  
 
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