Rare monogenic causes of steatotic liver disease masquerading as MASLD

Martijn Cgj Brouwers*, David Cassiman

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
JournalJournal of Hepatology
DOIs
Publication statusE-pub ahead of print - 6 Mar 2024

Keywords

  • Diagnosis
  • Familial partial lipodystrophy
  • Glycogen storage disease
  • Hereditary fructose intolerance
  • NAFLD
  • Steatosis

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