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Spinal muscular atrophy type 3
Other Names for this Disease
- Kugelberg-Welander syndrome
- KWS
- Muscular atrophy, juvenile
- SMA 3
- SMA3
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Overview
These Web pages are updated as the Genetic and Rare Diseases Information Center
receives questions and as new information becomes available. If you don’t see
many information resources on this page, it may be because the Information Center
hasn’t yet received a question about this condition.
Your Questions Answered
by the Genetic and Rare Diseases Information CenterPlease contact us with your questions about Spinal muscular atrophy type 3. We will answer your question and update these pages with new resources and information.
On this page
General Information
- Families of SMA has created a booklet entitled Understanding SMA that is intended to serve as a source of information and support for children and adults with Spinal Muscular Atrophy (SMA).
- Genetics Home Reference (GHR) contains information on Spinal muscular atrophy type 3. Click on the link to go to GHR and review the information.
- Medscape Reference provides information on this topic. Click on the link to view this information. You may need to register to view the medical textbook, but registration is free.
- The National Institute of Neurological Disorders and Stroke (NINDS) collects and disseminates research information related to neurological disorders. Click on the link to view information on this topic.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge. Click on the link to read information on this topic.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Spinal muscular atrophy type 3. Click on the link to view a sample search on this topic.
- The The Online Mendelian Inheritance in Man (OMIM) database contains genetics resources that discuss Spinal muscular atrophy type 3. Click on the link to go to OMIM and review these resources.
