File:40265 2022 1735 Fig2 HTML.webp
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Summary
| Description |
English: Schematic of treatment for patients with primary hyperoxaluria (PH). If diagnosis is suspected, all patients with PH must be given the standard treatment of care by means of hyperhydration and citrate medication. In addition, patients with PH type 1 (PH1) should receive vitamin B6 (Vit B6) until a genetic diagnosis is available. With a genetic diagnosis in hand, the therapeutical processes are depicted in the figure. AKF acute kidney failure, ESKD end-stage kidney failure, PH2 PH type 2, PH3 PH type 3, RNAi RNA interference, Tx transplantation. *Missense mutations that respond to VitB6: p.G170R, p.G41R, p.F152I |
| Date | |
| Source | https://link.springer.com/article/10.1007/s40265-022-01735-x |
| Author | Bernd Hoppe & Cristina Martin-Higueras |
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English: This file is licensed CC BY-NC 4.0
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| current | 18:23, 26 September 2023 | | 685 × 996 (70 KB) | Ozzie10aaaa (talk | contribs) | Uploaded a work by Bernd Hoppe & Cristina Martin-Higueras from https://link.springer.com/article/10.1007/s40265-022-01735-x with UploadWizard |
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