HCU Network America’s Rare X HCU Data Collection Program Facebook Live Chat: Oral Health Survey Webinar

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Rare X HCU Data Collection Program Facebook Live Chat: Oral Health Survey Webinar November 17, 2022 From short roots to crowding of teeth, patients with various types of homocystinuria experience…

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HCU Network America’s Classical HCU Virtual Meet-Up

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Classical HCU Virtual Meet-Up October 9, 2022 Meetups are an opportunity to connect patients and caregivers impacted by Classical Homocystinuria to one another virtually. About this event Struggling with the…

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Webinar: Improving Classical Homocystinuria Outcomes Through Newborn Screening
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Webinar: Improving Classical Homocystinuria Outcomes Through Newborn Screening

On September 8, 2022, HCU Network America, a Patient Worthy partner organization, hosted a webinar program titled "Classical Homocystinuria: A Journey to Improve Outcomes Through Newborn Screening Methodology." The webinar…

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HCU Network America’s Classical HCU Virtual Meet-Up

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Classical HCU Virtual Meet-Up August 21, 2022 Meetups are an opportunity to connect patients and caregivers impacted by Classical Homocystinuria to one another virtually. About this event Struggling with the…

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HCU Network America Partners With RARE X to Create a Patient Registry
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HCU Network America Partners With RARE X to Create a Patient Registry

Patient Worthy partner HCU Network America and RARE X, a rare disease patient data service organization, have recently partnered in order to create a registry of patients living with homocystinuria,…

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