Webinar: The Role of Pathology in Diagnosing Lysomal Acid Lipase Deficiency (LAL-D)
Presented by: Dr. Subrata Chakrabarti, Chair, Department of Pathology and Laboratory Medicine at Western University and Chief of Pathology and Laboratory Medicine at London Health Sciences Centre & St. Joseph’s Health Care, London, Ontario, Canada.
Lysosomal Acid Lipase Deficiency (LAL-D) is an autosomal recessive lysosomal storage disorder [previously known as Wolman Disease (infants) and Cholesteryl Ester Storage Disease (children and adults)]. In pediatric and adult patients, nearly 50% progress to fibrosis, cirrhosis or liver transplant within 3 years of onset of symptoms.
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