Clinical Genetics is the diagnosis and management of genetic disorders affecting individuals and their families. The rapid increase in understanding of biological variation and its role in health and disease make it an exciting and expanding specialty. The training programme in clinical genetics is normally four years as a Specialty Registrar and research experience is actively encouraged.
Clinical genetic services run on a ‘hub and spoke' principle with central and district counselling services. There is close team working between Consultants, SpRs/StRs and Genetic Associates as well as interaction with cytogenetic and molecular laboratory colleagues. Members of the SAC in Clinical Genetics welcome queries from those considering a career in clinical genetics.
Entry into Clinical Genetics training is possible following successful completion of both a foundation programme and a core training programme There are three core training programmes for Clinical Genetics training:
We have completed our consultation on the new curriculum for Clinical Genetic. The new curriculum will be implemented in August 2021.
The curriculum for each specialty defines the process of training and the competencies needed for the award of a certificate of completion of training (CCT). The curriculum includes the assessment system for measuring trainees’ progress comprising workplace based assessment and knowledge based assessment.
A new Clinical Genetics curriculum will be implemented in 2021.
The Royal College of Pathologists provides the Certificate Examination in Medical Genetics and further information is available on the RCPath website.
Previous versions of the curriculum are no longer available online but copies can be requested from firstname.lastname@example.org.
The ARCP decision aid for each specialty defines the targets that have to be achieved for a satisfactory ARCP outcome at the end of each training year. The ARCP decision aid has been revised to reflect the curriculum changes approved in 2016 and replaces the previous version.