Industry Session by Inozyme Pharma: ENPP1 Deficiency: The Life-long Burden of a Rare Genetic Mineralization Disorder*

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Title: ENPP1 Deficiency: The Life-long Burden of a Rare Genetic Mineralization Disorder

This session will review the pathophysiology, clinical presentation, and diagnosis of ENPP1 Deficiency, a genetic disorder with evolving phenotypes across the age spectrum. We will discuss new data from a comprehensive ENPP1 Variants curation project and highlight current and emerging therapies in development.

Speaker:

  • Kurt Gunter, MD, Chief Medical Officer, Inozyme Pharma


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Industry Thought Leadership Session: Inozyme Pharma
11/16/2022 at 3:00 PM (EST)  |  Recorded On: 11/16/2022  |  35 minutes
11/16/2022 at 3:00 PM (EST)  |  Recorded On: 11/16/2022  |  35 minutes ENPP1 Deficiency: The Life-long Burden of a Rare Genetic Mineralization Disorder