The Struggling Odyssey of Infantile Primary Hyperoxaluria
Introduction: Oxalate overproduction in Primary Hyperoxaluria type I (PH1) leads to progressive renal failure and systemic oxalate deposition. In severe infantile forms of PH1 (IPH1), end-stage renal disease (ESRD) occurs in the first years of life. Usually, the management of these infantile forms i...
Saved in:
Main Authors: | Adrien Guillaume (Author), Benedetta Chiodini (Author), Brigitte Adams (Author), Karin Dahan (Author), Georges Deschênes (Author), Khalid Ismaili (Author) |
---|---|
Format: | Book |
Published: |
Frontiers Media S.A.,
2021-04-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Case Report: Sustained Efficacy of Lumasiran at 18 Months in Primary Hyperoxaluria Type 1
by: Benedetta Chiodini, et al.
Published: (2022) -
Case Report: Neonatal Unexplained HUS Treated With Complement Inhibitor Eculizumab
by: Dorottya Kelen, et al.
Published: (2021) -
Primary Hyperoxaluria in Korean Pediatric Patients
by: Yunsoo Choe, et al.
Published: (2019) -
Type 1 primary hyperoxaluria in a male infant
by: Benjamin Waddell, et al.
Published: (2017) -
Unusual cause of renal failure in infancy: Primary hyperoxaluria
by: Kanchan Channawar, et al.
Published: (2015)