ISMRD offers the following external sites for their potential usefullness in understanding Glycoprotein Storage Diseases. However, a listing here is not to be construed as an endorsement of that site's content by ISMRD and its Board of Directors.
Find diagnostic laboratories performing molecular and DNA analysis for establishing an initial diagnosis.
- Australia: National Referral Laboratory
- Norway: University Hospital of Northern Norway
- United States: Baylor College of Medicine | Greenwood Genetic Center | Institute of Genomic Medicine (UMDNJ) | Hayward Genetics Center, Tulane University
Sites that explain or perform prenatal testing.
- Kid’s Health for Parents
- Gene Tests International Clinic Directory
- Greenwood Genetic Center (US)
- Human Genome Project: Gene Testing
- March of Dimes: Prenatal Testing
- Mayo Clinic: Benefits and Risks of Genetic Tests
- Pacific Fertility Center (US)
- US National Library of Medicine
Investigation of new therapeutic techniques for Glycoprotein Storage Diseases and their underlying causes has accelerated in this new millennium. The following sites may be explored for monitoring this activity’s impact on Glycoprotein Storage Diseases.
- ClinicalTrials.gov: the National Institutes of Health's index of clinical trials proposed, under way and terminated.
Organizations & Agencies
- Coriell Institute
- National Ataxia Foundation
- National Center for Complimentary & Alternative Medicine
- National Institute of Child Health & Development
- National Institute of Dental & Craniofacial Research
- National Institute of Neurological Diseases & Stroke
- Office of Rare Diseases
- Society for the Study of Inborn Errors of Metabolism
- National Office for Rare Disorders
- Global Genes Project
- EveryLife Foundation
- EURORDIS: The voice for Rare Disease Patients in Europe
- Genetic Alliance
Current therapies for Glycoprotein Storage Diseases are primarily supportive or palliative in nature. However, bone marrow and cord blood transplantation have shown initial success for patients with Alpha-Mannosidosis and Fucosidosis. Enzyme Replacement Therapy is currently in phase III clinical trials for Alpha-Mannosidosis.
Bone Marrow & Cord Blood Transplants
- BMT Resources: Information assembled for the lay person by a five-time transplant recipient
- Cord Blood Donor Foundation
- Genetic Disease Treatment Options: University of California San Francisco transplant program's information on options for Lysosomal Diseases
- National Cord Blood Program
- National Marrow Donor Program
- Robert's Road to Recovery: Kathleen King's online journal about her son, Robert's, two transplants for Alpha-Mannosidosis.
- Ronald McDonald House Charities: Ronald McDonald Houses provide housing support internationally for families with a relative receiving a transplant
- Transplant Center Search: find a North American transplant center via BMT Infonet
Enzyme Replacement Therapy (ERT)
- Efficacy of ERT In Mice with Alpha-Mannosidosis
- The Hue-Man Project: A European collaborative effort to develop an effective enzyme replacement therapy for Alpha-Mannosidosis
- Zymenex: Scandinavian biopharmaceutical company currently engaged in the late stage pre-clinical development of a pharmaceutical intervention for Alpha-Mannosidosis