Identification of low gamma-glutamyl transferase familial intrahepatic cholestasis - benign recurrent intrahepatic cholestasis in a 22-year-old woman: A case report and literature review
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cholestasis
BRIC
PFIC
jaundice
low GGT

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Kamińska, M., Klapaczyński, J., Ołdakowska-Jedynak, U., & Kamińska, D. (2022). Identification of low gamma-glutamyl transferase familial intrahepatic cholestasis - benign recurrent intrahepatic cholestasis in a 22-year-old woman: A case report and literature review. Kwartalnik Naukowy Fides Et Ratio, 51(3), 141-145. https://doi.org/10.34766/fetr.v3i51.1099
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https://doi.org/10.34766/fetr.v3i51.1099
pdf (English)

Bibliografia

Ermis, F., Oncu, K., Ozel, M., et al. (2010). Benign recurrent intrahepatic cholestasis: late initial diagnosis in adulthood, Annals of Hepatology, 9, 207-210.

Gupta, V., Kumar, M., Bhatia, B.D. (2005). Benign recurrent intrahepatic cholestasis, Indian Journal of Pediatrics, 72, 793-794. https://rarediseases.org/rare-diseases/low-gamma-gt-familial-intrahepatic-cholestasis

Luketic, V,A., Shiffman, M,L. (2004). Benign recurrent intrahepatic cholestasis, Clinical Liver Disease, 133-149.

Ołdakowska-Jedynak, U., Jankowska, I., Hartleb, M., et al. (2014). Treatment of pruritus with Prometheus dialysis and absorption system in a patient with benign recurrent intrahepatic cholestasis, Hepatology Research, 44, E304-308.

Sohn, M.J., Woo, M.H., Seong, M.W., et al. (2019). Benign Recurrent Intrahepatic Cholestasis Type 2 in Siblings with Novel ABCB11 Mutations, Pediatric Gastroenterology, Hepatology and Nutrition, 22, 201–206. https://doi.org/10.5223/pghn.2019.22.2.201

Summerskill, W.H., Walshe, J,M. (1959). Benign recurrent intrahepatic ‘obstructive’ jaundice, Lancet, 2, 686–690.

Tygstrup, N., Jensen, B. (1969). Intermittent intrahepatic cholestasis of unknown etiology in five young males from the Faroe Islands, Acta Medica Scandinavica, 185, 523–530.

van Ooteghem, N.A., Klomp, L.W., van Berge Henegouwen, G.P., et al. (2002). Benign recurrent intrahepatic cholestasis progressing to progressive familial intrahepatic cholestasis: low GGT cholestasis is a clinical continuum, Journal of Hepatology, 36, 439-443.

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