Combined liver-kidney transplantation and follow-up in primary hyperoxaluria treatment: Report of three cases

Kavukcu, SALİH; Turkmen, M.; Soylu, A.; Kasap, B.; Ozturk, YEŞİM; Karadernir, S.; Bora, SEYMEN; Astarcloglu, I.; Gulay, H.

doi:10.1016/j.transproceed.2007.11.003

Combined liver-kidney transplantation and follow-up in primary hyperoxaluria treatment: Report of three cases

Atıf İçin Kopyala

Kavukcu S., Turkmen M., Soylu A., Kasap B., Ozturk Y., Karadernir S., ...Daha Fazla

TRANSPLANTATION PROCEEDINGS, cilt.40, sa.1, ss.316-319, 2008 (SCI-Expanded)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 40 Sayı: 1
Basım Tarihi: 2008
Doi Numarası: 10.1016/j.transproceed.2007.11.003
Dergi Adı: TRANSPLANTATION PROCEEDINGS
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.316-319
Dokuz Eylül Üniversitesi Adresli: Evet

Özet

Introduction. Primary hyperoxaluria type-1 (PHI) is an autosomal recessive disorder caused by impaired activity of the hepatic peroxisomal alanine-glyoxilate aminotransferase, which leads to end-stage renal disease (ESRD) and requires combined liver-kidney transplantation (CLKT). Herein, we have reported 3 children diagnosed with PHI who received CLKT.