Explore articles tagged with "Genetic and Syndromic Disorders"
Pompe disease is a rare genetic disorder affecting muscles and organs. Learn its symptoms, causes, treatment options and management for better health.
Fabry disease is a rare genetic disorder causing enzyme deficiency, organ damage and severe symptoms. Learn about causes, signs and treatment options.
Holt-Oram Syndrome is a rare genetic disorder causing heart and limb defects. Learn symptoms, diagnosis, treatment and long-term management insights.
Noonan Syndrome is a genetic disorder affecting growth and development. Learn about its symptoms, causes, diagnosis, and treatment options.
Turner syndrome (associated heart defects) impacts health with unique risks. Learn symptoms, causes, diagnosis, and treatments for better outcomes.
Down Syndrome (associated heart defects) poses unique challenges in diagnosis, treatment, and care. Learn insights to support better health outcomes.
Ehlers-Danlos Syndrome (Vascular Type) is a rare genetic disorder causing fragile blood vessels, risks, and unique challenges in care and treatment.
Loeys-Dietz syndrome is a rare genetic disorder affecting connective tissue, with serious cardiovascular risks, requiring diagnosis and treatment.
Marfan syndrome affects connective tissue, leading to heart, eyes, and skeletal complications. Learn causes, symptoms, diagnosis, treatment options.