Clinicopathological features of genetically confirmed Danon disease

Neurology. 2002 Jun 25;58(12):1773-8. doi: 10.1212/wnl.58.12.1773.

Abstract

Background: Danon disease is due to primary deficiency of lysosome-associated membrane protein-2.

Objective: To define the clinicopathologic features of Danon disease.

Methods: The features of 20 affected men and 18 affected women in 13 families with genetically confirmed Danon disease were reviewed.

Results: All patients had cardiomyopathy, 18 of 20 male patients (90%) and 6 of 18 female patients (33%) had skeletal myopathy, and 14 of 20 male patients (70%) and one of 18 female patients (6%) had mental retardation. Men were affected before age 20 years whereas most affected women developed cardiomyopathy in adulthood. Muscle histology revealed basophilic vacuoles that contain acid phosphatase-positive material within membranes that lack lysosome-associated membrane protein-2. Heart transplantation is the most effective treatment for the otherwise lethal cardiomyopathy.

Conclusions: Danon disease is an X-linked dominant multisystem disorder affecting predominantly cardiac and skeletal muscles.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adolescent
  • Adult
  • Antigens, CD / genetics*
  • Cardiomyopathies / enzymology
  • Cardiomyopathies / genetics
  • Cardiomyopathies / pathology
  • Child
  • Female
  • Humans
  • Intellectual Disability / enzymology
  • Intellectual Disability / genetics
  • Intellectual Disability / pathology
  • Lysosomal Membrane Proteins
  • Lysosomal Storage Diseases / enzymology
  • Lysosomal Storage Diseases / genetics*
  • Lysosomal Storage Diseases / pathology
  • Male
  • Membrane Glycoproteins / deficiency*
  • Membrane Glycoproteins / genetics*
  • Middle Aged
  • Muscle, Skeletal / enzymology
  • Muscle, Skeletal / pathology
  • Mutation / genetics
  • Pedigree

Substances

  • Antigens, CD
  • Lysosomal Membrane Proteins
  • Membrane Glycoproteins