Ampelokipoi 210-6983 222 | 213-0312 000
Gizi 216-070 0000

Online Digital Exam Portfolio

Display – print the test results of the desired referrer – command

Give, with absolute security, access to the third parties you wish

Non-syndromic hearing loss

Non-syndromic hearing loss

Childhood hearing loss is common - around one per 1,000 children suffer from severe or very severe hearing loss either from birth or during early childhood (preschool deafness).

More than half of the cases are caused by gene-inherited mutations.

Of the inherited situations, 70-80% are non-syndromic, without symptoms or dysfunctions in other organs of the body. Mutations, which are associated with varicocele are mainly found in the CX gene

Check Up Medicus | Non-Syndromic Hearing Loss | Prenatal molecular testing in inherited deafness. We receive samples Nationwide.

Genetic testing is recommended as a part of the woman's preventive prenatal check-up.

The results determine the need or not for:

  1. extra laboratory testing of the spouse in the CX gene
  2. fetal screening in case of the husband has a CX mutation


In our laboratory, analysis of individual gene mutations or overall analysis of the relevant gene is carried out.

The available tests are:

  1. Detection of CX 26 35delG base mutation
  2. Detection of 2 mutations (CX 26 35delG + L90P)
  3. Full analysis of the CX26 gene by Full Sequencing technique

Pay attention!

It is always important to consult a qualified healthcare professional before having any genetic testing to make sure you fully understand the conditions being tested for, as well as the interpretation of the results



A simple blood test is required for laboratory testing.

No preparation or diet is required. Blood sampling can be done at any time of the day.


Blood sampling can be done at any time of the day (laboratory hours 7.30 a.m. – 7.30 p.m.).


Results are given within 12 working days.


According to our latest update to EOPYY, it is NOT prescribed

The costs for the packages are:
  1. Basic mutation detection CX 26 35delG at 60 euros.
  2. Detection of 2 mutations (CX 26 35delG + L90P) at 100 euros.
  3. Full analysis – Full sequencing CX26 at 200 euros.

Information selected - indicative with sources: Interpretation of Diagnostic Tests - J.Wallach and

The choice and explanation of the use of the analysis is the exclusive responsibility of your doctor

Edited by : Ioannis Grattisia Head of Laboratory / MSc Clinical Biochemistry - Molecular Biology

2022 - 2023

Biopathology Diagnostic Laboratory | Microbiological | Molecular | DNA | Ultrasonic | EOPYY – Clinic

Diagnostic: Director Biochemist I. Gratsia - Biopathologist I. Katsavochristos / M. Kolokouri - Radiologist S. Alagiannis

Doctors: General Practitioner X. Chrysanthaki - Endocrinologist E. Typhoxylou – Cardiologist A. Castanas - Neurologist C. Karagiorgis - Urologist K. Psyllias - Pulmonologist Zafiria Barbaressou

Liability & Responsibility Ethics in Biomedical Science - Personalised Medical Practice with Courtesy and Empathy

Top 5-star examinee satisfaction performance in users via Google / Doctor any Time

Quality in diagnostic tests

Personal Data Security GDPR

e - Dating via Doctor Anytime at: Cardiologist - Urologist - Neurologist -Laboratory Diagnostic Examinations

News Blogs: - -

Biopathology Diagnostic Center – Athens | Medical Center Check Up Medicus | Checkup – Blood tests – EOPYY.

Contact us

Send us an email or call us in order to plan an appointment with a doctor or for a health check-up.

Check Up Medicus | Medical Center Athens | Blood Tests | Covid-19 Test
Compare items
  • Total (0)