Description
The Rare Links webinar series aims to provide a platform where national and international experts can share their knowledge and experience of developed and developing newborn screening programs in and approaches to developing this in Pakistan. At the end of this CME session, through interactive case based discussions the participants will be able to:
• Understand the clinical utility of newborn screening testing of rare inherited metabolic disorders
• Describe the tests for follow up testing of these rare disorders
• Interpret newborn screening tests and second tier tests through case discussions
To register use this link: https://docs.google.com/forms/d/1alE5NWwjLjRc_2h1jLG9dm4h7uP6FJLeLMEYaZkwRU8/viewform?edit_requested=true
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