DentalScan®

DentalScan®

Reveals the risk of periodontitis

Periodontitis is an inflammatory disease of the supporting structure for the teeth called the periodontium. The cause is a combination of the presence of certain strains of bacteria in dental plaque and the immunological or genetic predisposition of the patient. The DentalDUO bacterial and genetic examination detects both of the above-mentioned risk factors for periodontitis, which can significantly contribute to early diagnosis, the selection of optimal treatment or the adoption of appropriate preventive measures.

DentalScan®
3 200 Kč
DentalBAC
1 800 Kč
WHEN DO I RECEIVE THE RESULT?

WHEN DO I RECEIVE THE RESULT?

Within 15 working days after receipt of your sample.

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HOW THE SAMPLE IS TAKEN

HOW THE SAMPLE IS TAKEN

By gingival swab at your dentist's office.

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FREQUENTLY ASKED QUESTIONS

FREQUENTLY ASKED QUESTIONS

An overview of your most frequently asked questions and our answers.

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IN WHICH SITUATIONS IT IS APPROPRIATE TO TAKE THE TEST

DETAILED INFORMATION

DETAILED INFORMATION

Periodontitis affects up to one third of the population in various forms. It is caused by untreated inflammation of the gums or the supporting structure for the teeth, which can lead to the development of chronic inflammation of the oral cavity, tooth loss, increased risk of secondary infection of the body, heart attack, stroke and in women increases the risk of miscarriage or premature birth. Periodontitis is like most other diseases, the earlier it is diagnosed and treated, the better the patient's chances of recovery.

In the beginning, the disease may be relatively unnoticeable and painless. Typical symptoms that should not be overlooked include bleeding gums when brushing, sensitive or exposed tooth necks, bad breath or wobbling teeth. The most effective prevention is thorough dental and oral hygiene and regular preventive check-ups. As a preventive measure, you can undergo a DentalDUO examination, which detects the presence of periodontitis-causing bacterial strains and the genetic make-up of the patient, including the reactivity of the patient's immune system, which can significantly contribute to reducing the risk of serious complications.

The DentalDUO test consists of two parts. The DentalBac test (can be ordered separately) detects the presence of bacterial factors involved in the development of periodontitis, which can significantly contribute to early diagnosis, the choice of optimal treatment or the adoption of appropriate preventive measures. It detects 12 basic paropathogenic bacteria:

  • Highly pathogenic types:Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Treponema denticola, Tannerella forsythia, Filifactor alocis
  • Moderately pathogenic types: Prevotella intermedia, Parvimonas micra, Fusobacterium sp., Campylobacter rectus
  • Low pathogenic types: Eikenella corrodens, Capnocytophaga gingivalis, Eubacterium nodatum

The second part of DentalGEN identifies a patient's genetic predisposition to the risk of periodontitis, which can significantly contribute to early diagnosis, selection of optimal treatment or adoption of appropriate preventive measures.

You will receive the result within 15 working days.
HOW THE TEST WORKS AND WHAT YOU CAN EXPECT

HOW THE TEST WORKS AND WHAT YOU CAN EXPECT

After ordering the test, you will receive an email with detailed information. A DNA sample is obtained by swabbing the gingival sulcus. The sample is taken by a dentist using a sampling kit, which will be sent to you by post together with instructions and other documents. The result of the analysis will be communicated to you by telephone and we will agree how you wish to obtain the laboratory report. In case of a positive result, we will arrange a consultation with a geneticist who will explain everything and recommend appropriate measures. 

Frequently Asked Questions

The time required for the laboratory examination (sample analysis) and the delivery date of the result vary according to the type and complexity of the examination. Usually it is in the order of weeks, for complex tests up to several months. The delivery date of the result is indicated in the details of each test on our website. In urgent situations, e.g. for a woman with a newly diagnosed breast or ovarian tumour before surgery, the oncopanel cancer test is performed in STATIM mode and the result is available within 3-4 weeks, whereas in normal mode it takes up to 6 months.
Health insurance always covers genetic consultations recommended by the attending physician (usually a general practitioner, paediatrician, oncologist, gynaecologist or other specialist). During the consultation, a clinical geneticist will assess whether the indication criteria for testing for the predisposition genes are met; if so, the entire genetic test, including laboratory analysis of the sample and subsequent consultation with the geneticist/doctor, is covered by health insurance. If the criteria for the genetic testing are not met, the patient can pay for the selected/recommended test as a self-payment.
After making an appointment, you will come to our office where you will first fill out a personal and family history questionnaire, or you can download it from here on our website and fill it out in advance, in the comfort of your own home. Remember to bring it with you afterwards. This is followed by a consultation with a doctor who will compile your three-generation family tree and decide on the indication for laboratory genetic testing. We also recommend that you bring medical reports from recent important examinations.
Recommendation - a referral from the doctor who recommended the genetic consultation. Alternatively, a completed genetic family and personal history questionnaire, which can be downloaded here. However, the questionnaire can also be completed after you arrive at our office. Medical reports from previous examinations related to the requested genetic test. It is not necessary to be fasting for the genetic examination, so you can easily make an appointment in the afternoon.
By phone at 800 390 390 or 234 280 280, by e-mail at info@ghcgenetics.cz.
It has been reported that approximately 5-10% of cancers are caused by inborn changes in certain genes. One of the main goals of predictive genetic testing is the early identification of people at risk. If risk predispositions (gene mutations) are detected, preventive follow-up at specialised centres is recommended, where possible cancers are detected early and the chances of successful treatment are increased. In the case of high-risk mutations, preventive surgery may be recommended to make the risk of cancer in a given organ virtually impossible (for example, removal of the breast glands or removal of the uterus and ovary in BRCA1 or BRCA2 mutation carriers).
If your first-degree relative (parents, siblings, children) develops colon cancer before the age of 45, your risk of developing this cancer is 5 times higher. If you have three first-degree relatives, your risk can be as high as 50%. In families with a history of recurrent bowel cancer or with a history of bowel cancer at a young age, it could be hereditary cancer syndrome (Lynch syndrome). In such cases, genetic consultation is recommended.

Do you have a question or don't know which test to choose?

Call us at 800 390 390 or contact us and we'll be happy to help.