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Tropheryma whipplei, Molecular Detection

Includes 1 test

Molecular screening for Tropheryma is used to diagnose Whipple disease, especially to detect ambiguous or suspicious cases.

More information

Whipple disease is a chronic, systemic disease that in most cases involves the small intestine and its lymphatic tissue. The disease mainly affects middle-aged men, with an increased incidence in the third and fourth decade of life. Clinical findings may include malabsorption, chronic diarrhea, abdominal pain, arthralgia, fever, and central nervous system symptoms. The disease is due to the bacterium Tropheryma whipplei (formerly called Tropheryma whippelii) of the Radiobacterium family. The microbe is stick-shaped and does not stain Gram.




Important Note

Laboratory test results are the most important parameter for the diagnosis and monitoring of all pathological conditions. 70%-80% of diagnostic decisions are based on laboratory tests. Correct interpretation of laboratory results allows a doctor to distinguish "healthy" from "diseased".

Laboratory test results should not be interpreted from the numerical result of a single analysis. Test results should be interpreted in relation to each individual case and family history, clinical findings and the results of other laboratory tests and information. Your personal physician should explain the importance of your test results.

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Additional information
Tests includedIncludes 1 test
Sample Blood
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