Global

Rare Disease Education:  PGAP3-Congenital Disorder of Glycosylation

Editor: Kelsey LaFayette, DNP, RN, FNP-C

This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Rare Disease Education: Shwachman-Diamond Syndrome

This content aligns with Goal 3: Good Health and Wellbeing by outlining approaches for diagnosing HIV in infants, children, adolescents, and young adults and providing an overview of the pathologic effects of HIV on various organ systems in these age groups.

This content aligns with Goal 3: Good Health by addressing Fragile X syndrome (FXS), a significant cause of intellectual disability, and exploring potential treatments that could improve health outcomes for affected individuals through the restoration of gene function. Additionally, it aligns with Goal 10: Reduced Inequalities by emphasizing the importance of understanding genetic and epigenetic factors in FXS, which can lead to more equitable healthcare options and targeted interventions for individuals with this condition, ultimately promoting inclusion and reducing disparities in health access and treatment.