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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Mucolipidosis III alpha/beta


Other Names for this Disease

  • ML 3 A
  • ML3
  • Mucolipidosis type 3A
  • Pseudo-Hurler polydystrophy
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Treatment

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Management Guidelines

  • GeneReviews provides current, expert-authored, peer-reviewed, full-text articles describing the application of genetic testing to the diagnosis, management, and genetic counseling of patients with specific inherited conditions. Click on the link to view the article on this topic.
  • Project OrphanAnesthesia is a project whose aim is to create peer-reviewed, readily accessible guidelines for patients with rare diseases and for the anesthesiologists caring for them. The project is a collaborative effort of the German Society of Anesthesiology and Intensive Care, Orphanet, the European Society of Pediatric Anesthesia, anesthetists and rare disease experts with the aim to contribute to patient safety.
Other Names for this Disease
  • ML 3 A
  • ML3
  • Mucolipidosis type 3A
  • Pseudo-Hurler polydystrophy
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.