News
Articles
GHC Genetics significantly supported the "Plešouni" project for children with cancer
The Plešouni project is a Czech charity educational multimedia project - an animated series (13 episodes) is being created, which explains to children in an understandable and sensitive way what to expect during treatment, how chemotherapy works or how to cope with psychologically challenging moments. The series is created with an emphasis on humour, empathy and playfulness, which helps children process complex emotions and information. In addition to the series, the project also includes a mobile and tablet app that serves as an interactive guide to treatment. GHC Genetics financially supported this project and adopted an important character within the bald identity - Captain CHEMO. He is the main sidekick to children going through challenging cancer treatments in their upcoming series.
Option to log in to your personal profile via Bank iD
Dear clients, starting today (May 30, 2025), you can log in to your personal profile on ghcgenetics.cz using the Bank iD service, which you are surely familiar with and use to communicate with your bank, government agencies, and other entities.
We have published a new article in the professional journal Acta medicinae on tumor syndromes.
In the latest issue of the journal Acta medicinae, Dr. Zděnka Vlčková, head of the clinical genetics department at GHC Genetics, published a comprehensive article on hereditary cancer syndromes.
We are recruiting a doctor for our genetic clinic
Professional requirements:
Doctor/physician with specialized competence in medical genetics or doctor/physician with completed basic tribe or graduate doctor.
The first year of the Czechoslovak Congress of Medical Genetics took place with our active participation.
On 2-4 April 2025, the first ever Czechoslovak Congress of Medical Genetics took place at the Elektra Cultural and Congress Centre in Luhačovice. This new platform builds on the long-standing cooperation of Czech and Slovak experts in the field of medical genetics and was created by combining two traditional events - the Martin Genetics Conference and the national DNA diagnostics conference.
The congress was well attended by experts from both countries and offered a rich professional programme, which included contributions from our colleagues. In total, there were 5 lectures from the team of GHC GENETICS SK, GHC GENETICS CZ and PRENET.
We would like to thank the entire author team for representing our companies and contributing to the expert discussion. We believe that the Czechoslovak Congress will become a regular platform for knowledge sharing and interdisciplinary collaboration.