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Editorial
. 2022 May;89(5):427-428.
doi: 10.1007/s12098-022-04128-w. Epub 2022 Mar 9.

Liver Transplantation for Tyrosinemia Type 1 in the Developing World: Is It Really the Best We Can Offer?

Rishi Bolia  1 , Anshu Srivastava  2
Affiliations
Editorial

Liver Transplantation for Tyrosinemia Type 1 in the Developing World: Is It Really the Best We Can Offer?

Rishi Bolia et al. Indian J Pediatr. 2022 May.
No abstract available

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References

    1. Menon J, Shanmugam N, Valamparampil JJ, et al. Liver transplantation: a safe and definitive alternative to lifelong nitisinone for tyrosinemia type 1. Indian J Pediatr. 2021. https://doi.org/10.1007/s12098-021-03826-1 . - DOI - PubMed
    1. Chinsky JM, Singh R, Ficicioglu C, et al. Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations. Genet Med. 2017. https://doi.org/10.1038/gim.2017.101. - DOI - PubMed - PMC
    1. Spiekerkoetter U, Couce ML, Das AM, et al. Long-term safety and outcomes in hereditary tyrosinaemia type 1 with nitisinone treatment: a 15-year non-interventional, multicentre study. Lancet Diabetes Endocrinol. 2021;9:427–35. - DOI
    1. Vimalesvaran S, Souza LN, Deheragoda M, et al. Outcomes of adults who received liver transplant as young children. E Clinic Med. 2021;38:100987.
    1. Mayorandan S, Meyer U, Gokcay G, et al. Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice. Orphanet J Rare Dis. 2014;9:107. - DOI

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