Preventive health care

OWING TO THE CONTINUOUS STRESS AND THE LACK OF LEISURE TIME MANY PERSONS VISIT THE APPROPRIATE MEDICAL SPECIALIST LATE, AND THEREFORE THE EARLY RECOGNITION AND TREATMENT OF DISEASES IS IMPOSSIBLE

By the organization of wide screening tests, our company is aimed at providing opportunities for basic and full medical specialists’ examinations to those who have little leisure time, but think in a health-conscious way and make every effort to live a quality life.

As part of the preventive health care programme, screening tests can be provided under civilized circumstances, with the inclusion of highly trained medical specialists, in clinics equipped with modern instruments, at the time chosen by patients, without waiting.

WE CAN SEND A DETAILED EXAMINATION PROGRAMME IF THIS NEED WAS INDICATED IN THE COURSE OF REGISTRATION.

GENERAL SCREENING PROGRAMMES

GENERAL SCREENING PROGRAMMES

MAXIMUM

Thorough Screening Test

OPTIMUM MANAGER SCREENING PACKAGE + OSTEODENSITY MEASUREMENT
DERMATOLOGY MEDICAL SPECIALIST EXAMINATION
CARDIAC ULTRASOUND EXAMINATION
UROLOGY TEST
THYROID ULTRASOUND EXAMINATION

120.350,-Ft

OPTIMUM

Manager Screening Test

FULL LABORATORY TEST
STOOL – BLOOD TEST (3X)
ABDOMEN AND TRUE PELVIS ULTRASOUND
GENERAL EXAMINATION IN INTERNAL MEDICINE AND CARDIOLOGY WITH ECG
SURGERY SPECIALIST EXAMINATION
OTORHINOLARYNGOLOGY EXAMINATION, HEARING TEST
OPHTHALMOLOGY SPECIALIST EXAMINATION
GYNAECOLOGY SPECIALIST EXAMINATION
UROLOGY EXAMINATION
SUMMARY OPINION AND CONSULTANCY

82.000,-Ft

MINIMUM

General Screening Test

DERMATOLOGY SPECIALIST EXAMINATION
OSTEODENSITY MEASUREMENT
CARDIAC ULTRASOUND EXAMINATION
GENERAL OVERVIEW SCREENING TEST
(ABDOMEN AND TRUE PELVIS ULTRASOUND, FULL LABORATORY, STOOL – BLOOD TEST (3X), INTERNAL MEDICINE)

48.650,-Ft

SCREENING OF HEREDITARY CANCER DISEASES

Our DNS diagnostic laboratory provides high-level genetic information synchronized with the most up-to-date data of the scientific literature in the field of both frequent hereditary diseases and the most frequent cancer-related diseases. In the course of the examinations we perform the diagnostics of hereditary diseases and provide help to specific treatment of cancer-related diseases, considerably improving the result.

Screening of hereditary diseases

Both genetic and environmental factors play an important role in the development and progress of numerous diseases. Significant demand is shown in particular for revealing the mutations of to be found in the CFTR gene causing propensity to cystic fibrosis, as well as in the BRCA1 and BRCA2 genes causing propensity to breast cancer (and ovary cancer). Our examinations provide for the analysis of the full coding region of the genes examined with the help of the new-generation DNS sequencing.

Material necessary for the examination: 5 millilitre EDTA blood, mouth mucosa smear or cleaned DNS.

Cystic fibrosis

Cystic fibrosis is one of the most frequent congenital disease. Its frequency is 1/2500-3000 in the white (Caucasian) population. In Hungary each 28th person is a carrier. The gene defect may remain hidden in families even through several generations, and only appears in the form of an illness if both parents carry the defective gene section.

Hereditary diseases

• Cystic fibrosis
• Hereditary breast and ovary cancer
• Individually tailored cancer therapy – tumour marker diagnostics

Individually-tailored cancer therapy, diagnostics of tumour markers

Revolutionary changes have recently occurred in the healing of cancer: preparations with target impacts have become achievable in the case of several cancer types, as a result of which in many cases improvement can be noticed in the condition of cancer patients. Based on the examination of tumour markers defined in the course of the individually-tailored therapy, the preparation to be used in the case of the individual patients can be determined.

The currently most efficient manner of the treatment of the colon, rectum and non-small cell lung tumours is aimed at the so-called EGFR signalling route. Examination of the following genes is recommended for the targeted therapy: KRAS, NRAS, EGFR, BRAF, PIK3CA, C-KIT. These examinations are performed with validated diagnostic kits marked CE IVD.

Screening of hereditary cancer diseases

THE COSTS OF EXAMINATIONS ARE DIFFERENT.

With knowledge of your examination requirement, we can provide you more information and a detailed
PRICE OFFER

hereditary cancer

diseases

Cystic fibrosis

Hereditary breast and ovary cancer

Individually tailored cancer therapy – tumour marker diagnostics

GENETIC SCREENING EXAMINATIONS

Hereditary breast and ovary cancer

In Hungary, breast cancer is the most frequent malignant tumour of women: there is a risk

of 10% in general population that a woman has breast cancer during her life. In a part of cases a hereditary gene irregularity (mutation) is responsible for the development of breast and ovary tumours. Approximately half of the hereditary mutations causing propensity to breast cancer can be found in the BRCA1 and BRCA2 genes. In case mutation is found in the above genes, there is a possibility of 50 to 90% that a tumour is developed in the person during her life.

Through the participation of a Hungarian-owned company co-operating with us in health care, we can offer gene diagnostic services, as a result of which the development of diseases can be prevented in an individually-tailored form. Based on a preventive gene diagnostic examination, an individually-tailored proposal is made to protect health, whose background shall be provided by the high-tech gene mapping laboratory.

Gene mapping is made on the basis of a mouth mucosa smear, simply, quickly and painlessly.

The costs of examinations are different!

With knowledge of your examination requirement, we can provide you more information and a detailed price offer!

GENE DIAGNOSTICS

CURRENT EXAMINATIONS

• Antioxidant gene map
• Osteodensity gene map
• Children conception gene map
• Tumour development gene map
• Dentistry gene map
• Cardiac and vascular gene map
• Nutrition gene map