NTBC and correction of renal dysfunction

Arianna Maiorana, Carlo Dionisi-Vici

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Hereditary tyrosinemia type 1 (HT1) is characterized by severe progressive liver disease and renal tubular dysfunction. Kidney involvement is characterized by hypophosphatemic rickets and Fanconi syndrome. Different animal models were useful to investigate the pathophysiology of the disease and the effects of NTBC therapy on liver and kidney function. NTBC has revolutionized the prognosis of HT1 and its acute and chronic effects on renal tubular function have been proved, with normalization of tubular function within a few weeks, particularly hypophosphatemia and proteinuria. NTBC therapy is highly effective in improving renal function both at short and long-term. However, its efficacy critically depends on the age at start of treatment with normal outcome in patients diagnosed at birth by newborn screening.

Original languageEnglish
Title of host publicationAdvances in Experimental Medicine and Biology
PublisherSpringer New York LLC
Pages93-100
Number of pages8
Volume959
DOIs
Publication statusPublished - Jan 1 2017

Publication series

NameAdvances in Experimental Medicine and Biology
Volume959
ISSN (Print)0065-2598
ISSN (Electronic)2214-8019

Keywords

  • Fanconi syndrome
  • NTBC therapy
  • Renal tubular dysfunction
  • Rickets

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

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