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The Liver and Lysosomal Storage Diseases: From Pathophysiology to Clinical Presentation, Diagnostics, and Treatment

Patryk Lipiński1, Anna Tylki-Szymańska2

  • 1Institute of Clinical Sciences, Maria Skłodowska-Curie Medical Academy, 00-136 Warsaw, Poland.

Diagnostics (Basel, Switzerland)
|June 27, 2024
PubMed

Keywords:
Gaucher diseaseNiemann–Pick type C diseaseacid sphingomyelinase deficiencyelevated transaminasesenzyme replacement therapyhepatomegalyliverliver fibrosisliver transplantationlysosomal acid lipase deficiencysplenomegaly

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