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Common genetic conditions – Practical genetics (1.5 CPD hours)

 

Full CPD module

 

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.

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