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Comment
. 2022 Aug;76(2):E45-E46.
doi: 10.1002/hep.32489. Epub 2022 Apr 15.

Letter to the editor: The burgeoning field of progressive familial intrahepatic cholestasis

Claudia Mandato  1 , Pietro Vajro  1
Affiliations
Comment

Letter to the editor: The burgeoning field of progressive familial intrahepatic cholestasis

Claudia Mandato et al. Hepatology. 2022 Aug.
No abstract available

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References

REFERENCES

    1. Mandato C, Zollo G, Vajro P. Cholestatic jaundice in infancy: struggling with many old and new phenotypes. Ital J Pediatr. 2019;45:83. https://doi.org/10.1186/s13052-019-0679-x
    1. Ibrahim SH, Kamath BM, Loomes KM, Karpen SJ. Cholestatic liver diseases of genetic etiology: advances and controversies. Hepatology. 2022;76:483-91.https://doi.org/10.1002/hep.32437
    1. Online Mendelian Inheritance in Man. Cassandra L. Kniffin. Cholestasis, Progressive Familial Intrahepatic 7, with or without hearing loss; PFIC7. Online Mendelian Inheritance in Man, OMIM®. Johns Hopkins University, Baltimore, MD. MIM Number: MIM Number: {619658}; {Date last edited: 12/10/2021}. World Wide Web URL: https://omim.org/
    1. Online Mendelian Inheritance in Man. Hilary J. Vernon. Cholestasis, progressive familial intrahepatic, 8; PFIC8. Online Mendelian Inheritance in Man, OMIM®. Johns Hopkins University, Baltimore, MD. MIM Number: {619662}; {Date last edited: 16/12/2021}. World Wide Web URL: https://omim.org/
    1. Mandato C, Siano MA, Nazzaro L, Gelzo M, Francalanci P, Rizzo F, et al. A ZFYVE19 gene mutation associated with neonatal cholestasis and cilia dysfunction: case report with a novel pathogenic variant. Orphanet J Rare Dis. 2021;16:179. https://doi.org/10.1186/s13023-021-01775-8

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