NirvanamKnowledge · Cases · Solver

Syndrome

Kartagener Syndrome

AMW:DIS:080014

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.

Pathology clinical
Read knowledge page ↗ Open graph Embed card

Graph assertions

Kartagener Syndrome has parent Bronchiectasis
Kartagener Syndrome has parent Ciliary Motility Disorders
Kartagener Syndrome has parent Dextrocardia
Kartagener Syndrome has parent Genetic Diseases, Inborn
Kartagener Syndrome has parent Respiratory System Abnormalities

Embed this node