Question

what is kartegener's syndrome explain fully

Answer 1

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Here is ur answer:

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Kartagener’s syndrome is a rare hereditary disease. It’s caused by a mutation that can occur on many different genes. It’s autosomal recessive, which means you must inherit a mutated gene from both of your parents to develop it.

Symptoms:

Kartagener’s syndrome involves two main characteristics: primary ciliary dyskinesia (PCD) and situs inversus. PCD can cause a number of symptoms, including:

♦ frequent respiratory infections

♦ frequent sinus infections

♦ frequent ear infections

♦ chronic nasal congestion

♦ infertility

Situs inversus doesn’t usually cause health problems.

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