Kartagener Syndrome

Overview

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.

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about Kartagener Syndrome

Topic type

Condition

Category

Cardiology

MeSH classification

C08.127.384.500|C08.200.531|C08.695.501|C09.150.531|C14.240.400.280.500|C14.280.400.280.500|C16.131.077.245.500.531|C16.131.240.400.280.500|C16.131.740.501|C16.131.810.250.500|C16.320.184.500.531|C16.320.480

Preparing for an appointment about Kartagener Syndrome

If you are speaking with a healthcare professional about Kartagener Syndrome, it can help to prepare a few details in advance.

• Write down your symptoms and when they started.
• Bring details of any medicines, supplements or previous treatments.
• Ask what tests or assessments may be needed.
• Ask what treatment or management options may be suitable.
• Ask when you should seek urgent medical help or follow-up care.

Finding care related to Kartagener Syndrome

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