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Close relative marriage, genetic risk and equitable access to clinical genomic services
The Close Relative (Consanguineous) Marriage programme supports healthcare professionals to better understand the genetic risks associated with close relative marriage and to improve equitable access to genomic information and services for affected families. The programme comprises multiple elearning sessions hosted on the NHS Learning Hub, with assessments and a downloadable certificate available on completion.
Intended audience
This learning is designed for:
- Health visitors
- Midwives
- GPs
- Paediatricians
- Social workers
- Public health practitioners
- Genetic counsellors
Key areas covered
Across the programme, learners will explore:
- National and local data on consanguinity and associated genetic risks
- Principles of genetic inheritance and recessive genetic disorders
- The impact of consanguinity on stillbirth, neonatal and infant mortality
- Approaches to improving access to genetic services for “at risk” families
- Best practice for communicating genetic information sensitively and effectively
- The role of this work in supporting Government ambitions to reduce infant deaths and health inequalities
Learning objectives
By completing the programme, learners will be able to:
- Review and interpret relevant data to deepen their understanding of this healthcare need
- Identify actionable ways to improve service quality and equity for affected families
- Build confidence in applying and sharing good practice principles with colleagues
- Reflect on new knowledge through integrated assessments
Learners may also wish to access the Genomics Education Programme, available in the Genomics in the NHS elearning catalogue on the Learning Hub.
This programme was originally located on the elfh hub and was first published on 3 March 2022. It migrated on to the Learning Hub on 23 May 2024.