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Danon disease (DD) is a rare, X-linked disorder associated with severe cardiomyopathy, and in many cases, skeletal myopathy, and cognitive impairment caused by mutations in the LAMP2 gene. There is still uncertainty regarding the natural history of DD because of its rarity.
This study aims to determine the natural history of DD through the collection and analysis of retrospective and prospective data. To achieve this, the investigators will perform surveys and obtain medical records from DD patients. The same cohort of patients will also be assessed by a multidisciplinary team with expertise in DD (cardiologist, neurologist, ophthalmologist, psychologist, geneticist) at the University of California, San Diego. All patients with DD are eligible, including those who underwent a heart transplant. Additionally, data and records from deceased patients will provide valuable retrospective data for this study.
Full description
The study design will include:
Collection of information for all patients from:
Collection of information from living patients assessed by the multidisciplinary team at the University of California, San Diego including:
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Inclusion criteria
• Living or deceased patients with a diagnosis of Danon disease(including patients who may or may not have undergone heart transplantation) based on a genetic test positive for the LAMP2 mutation
Exclusion criteria
• Patients without a genetic test positive for a LAMP2 mutation
200 participants in 2 patient groups
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Central trial contact
Eric Adler, MD
Data sourced from clinicaltrials.gov
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