PreSENTIA: Paraganglioma / Pheochromocytoma

Synonyms: -

Material:

Buccal swab

TAT:

2-3 weeks

Method:

NGS

Overview

Paraganglioma/Pheochromocytoma are rare types of tumours of the adrenal glands. They are considered as a subset of Neuroendocrine tuumors (NETs) and originate from specific cells of the neuroendocrine system. About 40% of the cases are linked to hereditary syndromes, which elevate the risk of developing cancer in the future.

PreSENTIA Paraganglioma/Pheochromocytoma cancer panel tests for numerous germline mutations in 6 genes that could cause paraganglioma or pheochromocytoma cancers in the future. Identifying germline mutations associated with cancer susceptibility empowers healthcare providers and patients, as it allows them to take better and more informed decisions.

PreSENTIA: Paraganglioma / Pheochromocytoma

6 Gene(s)*

RET

SDHAF2

SDHB

SDHC

SDHD

VHL

Who is the test for

How many hereditary cancer syndromes are associated with this panel

Recommendations by professional bodies

References

Created by

Our editorial team consists of medical specialists and scientists in the field of human genetics. All content is created and reviewed in accordance with current scientific standards.

Last Update : 01.10.2026

How to order a genetic test

Select the right test for your patients. Contact our team in case you do not have an active contract yet.

Collect the sample. Download and fill in the order and consent form or access our portal (available for sample sent to Germany).

Properly pack the sample and send it to Medicover Genetics.

The sample will be analysed in our accredited laboratories.

An actionable report will be available for you to access safely and securely.

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