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What is Gaucher disease? Visit GaucherDisease.info
Visit GaucherDisease.info to learn about the rare genetic disorder, Gaucher disease (or Gaucher’s). Symptoms include enlarged liver and spleen, bleeding and bruising, and joint pain.
고셔병이란? - GaucherDisease.kr
Visit GaucherDisease.info to learn about the rare genetic disorder, Gaucher disease (or Gaucher’s). Symptoms include enlarged liver and spleen, bleeding and bruising, and joint pain.
National Gaucher Foundation | Gaucher Disease - Symptoms, Treatment, & Education
Gaucher disease is a genetic disorder and affects the body's organs and tissues. Learn about Gaucher disease symptoms, testing and treatments.
Rare Genetic Obesity: Causes, Signs, Diagnosis - Uncommon Obesity
Learn more about rare genetic disorders of obesity, including dysfunction in a key pathway involved in hunger regulation, symptoms to look for, and options for diagnosis.
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Learn about Alzheimer's disease including symptoms, diagnosis, treatment, patient stories, & more.
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We are focused on the development of precision genetic medicines to treat rare neuromuscular and central nervous system diseases. Learn more about Sarepta.
Sarepta Therapeutics | Biopharmaceutical Company for Rare Diseases
We are focused on the development of precision genetic medicines to treat rare neuromuscular and central nervous system diseases. Learn more about Sarepta.
Sarepta Therapeutics | Biopharmaceutical Company for Rare Diseases
We are focused on the development of precision genetic medicines to treat rare neuromuscular and central nervous system diseases. Learn more about Sarepta.
knowHAE | Get to know hereditary angioedema (HAE)
Learn more about the rare disease hereditary angioedema (HAE), including signs and symptoms, how it’s diagnosed, treatment options, and more.
knowHAE | Iepazīt hereditāra angioedema (HAE)
Learn more about the rare disease hereditary angioedema (HAE), including signs and symptoms, how it’s diagnosed, treatment options, and more.
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Malaysian Rare Disorders Society (MRDS) We represent and look out for the welfare of individuals including their families that are affected by rare disorders. Learn More About MRDS Who We Are Malaysian Rare Disorders Society (MRDS) was formed in 2004, with the help and guidance of the Genetic Unit, Department of Paediatrics, University Malaya Medical […]
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Learn about periodic fever syndrome and rare autoinflammatory diseases including CAPS, SJIA, AOSD, FMF, TRAPS, HIDS/MKD and Gout. Understand the science, hear expert insights and read patient stories about what it is really like to live with the disease. Visit our website to learn more today.
hATTR Guide: Learn the Signs of Hereditary ATTR Amyloidosis
Learn about hereditary transthyretin amyloidosis (hATTR), a rare, life-threatening disease that often goes undiagnosed due to a constellation of seemingly unrelated red-flag symptoms like bilateral carpal tunnel syndrome, heart failure, neuropathic pain, and chronic GI distress.
Alzheimer's disease memoir: Fierce Blessing; Children's authors; School Visits; Screenplays
Terry & Wayne Baltz are the authors of the Alzheimer's caregiver memoir Fierce Blessing: A Journey into Alzheimer's, Compassion, and the Joy of Being, a memoir about Alzheimer's disease. Their books for young readers include The Invisible Kid series and Night Of The Falling Stars. They have visited nearly 80,000 children in schools in seven states with their program and books...
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