Genetic background for MALIGNANT THYROID TUMOURS

Test covers the analysis of
19850 genetic changes in 13 genes related:

  • follicular carcinoma,

  • papillary carcinoma,

  • microadenocarcinoma,

  • poorly differentiated thyroid carcinoma,

  • undifferentiated thyroid carcinoma,

  • medullary carcinoma.

POBIERZ SKIEROWANIE – uzupełnij i dołącz do materiału (KLIKNIJ)

4,690.00 

Why is it worth testing?

The waiting time for the result is only 4 weeks

The analysis always includes genetic changes within exons, introns and promoters of genes and in mitochondrial DNA

Always an additional test included in the price

Consultation with specialist and written interpretation of the result

Each result is reanalysed every 6 months .

Rough data from sequencing are made available on request.


Malignant thyroid tumours – are considerably rare and their early diagnosis is not easy.

In the first period malignant thyroid tumours do not differ from their benign form.

Thyroid cancer is 9th most common cancer in the world.

It is 5th most common malignant cancer in women and 16th in men.

In 2020 about 580 000 new cases were diagnosed.


The most common symptoms of thyroid cacer are:

♦ painful lump or swelling of the front of the neck,

♦ swelling of the lymph nodes of the neck,

♦ unexplained hoarseness,

♦ sore throat that does not go away,

♦ difficulty swallowing,

♦ breathing problems.

 

Every year in Poland about 2000 malignant thyroid cancers are diagnosed.

In Poland, in 2020, the mortality rate standardised by age

for males was 0.5/100,000 people

for women 0,4/100,000 people 0,4/100 000 osób

Risk factors:

♦ genetic load,

♦ genetic syndromes (FNMTC, Cowden, MEN2, MEN2b, familial adenomatous polyposis),

♦ female gender,

♦ age over 50,

♦ radiation therapy in the area of the neck,

♦ obesity,

♦ high content of iodine in diet,

♦ high levels of thyroid stimulating hormone (TSH).

Test covers the analysis of 19850 genetic changes (SNP) in 13 genes:

Ostatnia aktualizacja bazy: 2023.11.15

Still in doubt? Any questions?

We encourage you to contact us to resolve any doubts!
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