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Wolman disease: A rare inherited lipid storage disease. The condition usually results in death early in life. More detailed information about the symptoms, causes, and treatments of Wolman disease is available below.
See full list of 26 symptoms of Wolman disease
See full list of 7 treatments for Wolman disease
Read more about Deaths and Wolman disease.
Review possible medical complications related to Wolman disease:
Read more about causes of Wolman disease.
Research the causes of these diseases that are similar to, or related to, Wolman disease:
Medical research articles related to Wolman disease include:
Click here to find more evidence-based articles on the TRIP Database
Prognosis for Wolman disease: There is no treatment and death usually occurs during the first year of life.
More about prognosis of Wolman disease
Visit our research pages for current research about Wolman disease treatments.
The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Wolman disease include:
Read more about Clinical Trials for Wolman disease
Types of Wolman disease
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Severe infantile form of inherited lysosomal lipid storage disease due to deficiency of acid lipase; results in accumulation of neutral lipids, particularly cholesterol esters, within cells. - (Source - Diseases Database)
Wolman disease is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Wolman disease, or a subtype of Wolman disease,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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