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Updated: Feb 13, 2026

Defining Substrate Specificities for Lipase and Phospholipase Candidates
Published on: November 23, 2016
Lysosomal Acid Lipase Deficiency: Report of Five Cases across the Age Spectrum
Marco Antonio Curiati1, Sandra Obikawa Kyosen1, Vanessa Gonçalves Pereira2
1Reference Center for Inborn Errors of Metabolism (CREIM), Department of Pediatrics, Universidade Federal de São Paulo (UNIFESP), São Paulo, SP, Brazil.
Abstract:
Lysosomal acid lipase (LAL) deficiency is an autosomal recessive lysosomal storage disorder caused by mutations in the LIPA gene that leads to premature organ damage and mortality. We present retrospective data from medical records of 5 Brazilian patients, showing the broad clinical spectrum of the disease.
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