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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Neutral lipid storage disease with myopathy


Other Names for this Disease

  • Neutral lipid storage disease without ichthyosis
  • NLSDM
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Inheritance

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How is neutral lipid storage disease with myopathy inherited?

This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.[1]
Last updated: 5/8/2014

References
  1. Neutral lipid storage disease with myopathy. Genetics Home Reference (GHR). February 2014; http://ghr.nlm.nih.gov/condition/neutral-lipid-storage-disease-with-myopathy. Accessed 5/8/2014.


Other Names for this Disease
  • Neutral lipid storage disease without ichthyosis
  • NLSDM
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.