Ensure healthy lives and promote well-being for all at all ages
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: Nail-Patella 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 Anemia of Chronic Disease.
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 Epidermolysis Bullosa that can cause life-threatening infections as well as some forms of cancer.
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 Gorlin Syndrome, a mutation in a tumor suppressor gene is the root cause of proliferation of cancer cells, leading to basal cell carcinomas, abnormal cysts in the jaw, bone deformities, and several other manifestations.
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 Leprosy, an ancient chronic infection disease that can affect the skin, eyes, and nervous system.
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 Ovarian Cancer, a difficult to detect cancer in which only 2 in 10 cases are diagnosed at an early stage.
This podcast, relating to SDG 3, Health and Wellbeing, is part of the Elsevier celebration of the World Health Organization’s World Health Day whose aim is to promote health, keep the world safe and serve the vulnerable – so everyone, everywhere can attain the highest level of health and well-being. April 7th 2023 marks the WHO’s 75th anniversary of World Health Day, with a focus of improving public health for all.
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 Turner Syndrome, a condition characterized by a partial or complete loss of one of the two X chromosomes in females. The manifestations of this can be quite variable, resulting in infertility and/or distinctive physical features such as a short stature, webbed neck, or a “shield chest”.
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 Pierre-Robin Sequence, a rare congenital condition characterized by physical anomalies that result in making the newborn's breathing difficult.
This article related 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 Tetralogy of Fallot, the single most common form of congenital heart disease that causes cyanosis (bluish discoloration from lack of oxygen).
