Richner-Hanhart syndrome (tyrosinemia type II)

Cutis. 2017 Dec;100(6):E20-E22.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child Development
  • Diet Therapy / methods*
  • Female
  • Humans
  • Infant
  • Keratitis, Dendritic* / diagnosis
  • Keratitis, Dendritic* / etiology
  • Keratoderma, Palmoplantar* / diagnosis
  • Keratoderma, Palmoplantar* / etiology
  • Mutation
  • Patient Care Management / methods
  • Treatment Outcome
  • Tyrosine / blood*
  • Tyrosine Transaminase* / deficiency
  • Tyrosine Transaminase* / genetics
  • Tyrosinemias* / blood
  • Tyrosinemias* / diagnosis
  • Tyrosinemias* / genetics

Substances

  • Tyrosine
  • Tyrosine Transaminase