This content aligns with Goal 3: Good Health by raising awareness of chromosomal conditions and their associated health challenges, such as intellectual disabilities and other clinical features, which underscores the need for early diagnosis and appropriate medical care. By discussing the complexities of diagnosing these conditions, especially prenatally, it highlights the importance of accessible genetic testing and healthcare resources that can improve health outcomes for affected individuals and families. Additionally, it supports Goal 10: Reduced Inequalities by emphasizing the need for equitable access to diagnostic tools and services for all populations, ensuring that individuals with chromosomal conditions receive the necessary support and care regardless of their socioeconomic status or background.
This content aligns with Goal 3: Good Health by providing a thorough understanding of cerebral palsy (CP), including its neurodevelopmental origins, clinical manifestations, and the importance of early detection through standardized tools. By outlining guidelines for diagnosis and management, the chapter emphasizes the need for comprehensive care strategies that can improve health outcomes and quality of life for children with CP. Additionally, it supports Goal 10: Reduced Inequalities by highlighting the significance of accessible diagnostic and management resources that ensure all children, regardless of their circumstances, receive timely and equitable care, ultimately promoting better developmental outcomes and reducing disparities in healthcare access.
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: Reiter Syndrome
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: Brown-Sequard Syndrome
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: Fibromuscular Dysplasia
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: Canavan Disease
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: Autoimmune Polyglandular Syndrome Type I
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 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: Thoracic Outlet Syndrome
