Common genetic conditions – Practical genetics (1.5 CPD hours)
25 March 2013
This module uses primary care case histories to guide you through common genetic conditions you may encounter in practice, including:
- Familial hypercholesterolaemia - how to diagnose and family risk
- Polycystic kidney disease - diagnostic criteria
- Neurofibromatosis type 1 - mainstay of management
- Down’s syndrome - annual surveillance
Visit Pulse Reference for details on 140 symptoms, including easily searchable symptoms and categories, offering you a free platform to check symptoms and receive potential diagnoses during consultations.
