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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Amish infantile epilepsy syndrome


Other Names for this Disease

  • Epilepsy syndrome, infantile-onset symptomatic
  • GM3 synthase deficiency
  • Infantile-onset symptomatic epilepsy syndrome - developmental stagnation - blindness
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

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.
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Please contact us with your questions about Amish infantile epilepsy syndrome. We will answer your question and update these pages with new resources and information.

Basic Information

  • Genetics Home Reference (GHR) contains information on Amish infantile epilepsy syndrome. This website is maintained by the National Library of Medicine.

In Depth Information

  • Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. 
Other Names for this Disease
  • Epilepsy syndrome, infantile-onset symptomatic
  • GM3 synthase deficiency
  • Infantile-onset symptomatic epilepsy syndrome - developmental stagnation - blindness
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.