Complete Recovery of Oxysterol 7α-Hydroxylase Deficiency by Living Donor Transplantation in a 4-Month-Old Infant: the First Korean Case Report and Literature Review

J Korean Med Sci. 2018 Nov 22;33(51):e324. doi: 10.3346/jkms.2018.33.e324. eCollection 2018 Dec 17.

Abstract

Oxysterol 7α-hydroxylase deficiency is a very rare liver disease categorized as inborn errors of bile acid synthesis, caused by CYP7B1 mutations. As it may cause rapid progression to end-stage liver disease even in early infancy, a high index of suspicion is required to prevent fatal outcomes. We describe the case of a 3-month-old boy with progressive cholestatic hepatitis and severe hepatic fibrosis. After excluding other etiologies for his early liver failure, we found that he had profuse urinary excretion of 3β-monohydroxy-Δ5-bile acid derivatives by gas chromatography/mass spectrometry analysis with dried urine spots on filter paper. He was confirmed to have a compound heterozygous mutation (p.Arg388Ter and p.Tyr469IlefsX5) of the CYP7B1 gene. After undergoing liver transplantation (LT) from his mother at 4 months of age, his deteriorated liver function completely normalized, and he had normal growth and development until the current follow-up at 33 months of age. We report the first Korean case of oxysterol 7α-hydroxylase deficiency in the youngest infant reported to undergo successful living donor LT to date.

Keywords: Bile Acid Synthesis Defects; Bile Acids and Salts; Liver Transplantation; Oxysterol 7-alpha-hydroxylase.

Publication types

  • Case Reports

MeSH terms

  • Bile Acids and Salts / analysis
  • Cytochrome P450 Family 7 / genetics*
  • DNA Mutational Analysis
  • Gas Chromatography-Mass Spectrometry
  • Humans
  • Infant
  • Liver Failure / diagnosis
  • Liver Failure / genetics
  • Liver Failure / pathology
  • Liver Failure / therapy*
  • Liver Transplantation*
  • Living Donors
  • Male
  • Polymorphism, Single Nucleotide
  • Republic of Korea
  • Steroid Hydroxylases / genetics*
  • Steroid Metabolism, Inborn Errors / diagnosis
  • Steroid Metabolism, Inborn Errors / therapy

Substances

  • Bile Acids and Salts
  • Steroid Hydroxylases
  • Cytochrome P450 Family 7
  • CYP7B1 protein, human