Clinical characteristics, genetic profile and short-term outcomes of children with primary hyperoxaluria type 2: a nationwide experience-Reference-Cited by-同舟云学术

Clinical characteristics, genetic profile and short-term outcomes of children with primary hyperoxaluria type 2: a nationwide experience

Published:2023-11-02 Issue: Volume: Page:
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Krishnasamy Sudarsan,Deepthi Bobbity,Kamath Nivedita,Iyengar Arpana,Thomas Christy Cathreen,Uthup Susan,Saha Anshuman,Mathew Georgie,Agarwal Indira,Tiewsoh Karalanglin,Bhat Nowneet Kumar,Mandal Kausik,Krishnamurthy Sriram^ORCID

Funder

Department of Biotechnology (DBT), Government of India

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology and Child Health

Link

https://link.springer.com/content/pdf/10.1007/s00467-023-06200-9.pdf

Reference30 articles.

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2. Hoppe B (2012) An update on primary hyperoxaluria. Nat Rev Nephrol 8:467–475

3. Cochat P, Rumsby G (2013) Primary hyperoxaluria. N Engl J Med 369:649–658

4. Talati JJ, Hulton SA, Garrelfs SF, Aziz W, Rao S, Memon A, Nazir Z, Biyabani R, Qazi S, Azam I, Khan AH, Ahmed J, Jafri L, Zeeshan M (2018) Primary hyperoxaluria in populations of Pakistan origin: results from a literature review and two major registries. Urolithiasis 46:187–195

5. Garrelfs SF, Rumsby G, Peters-Sengers H, Erger F, Groothoff JW, Beck BB, Oosterveld MJS, Pelle A, Neuhaus T, Adams B, Cochat P, Salido E, Lipkin GW, Hoppe B, Hulton SA, OxalEurope Consortium (2019) Patients with primary hyperoxaluria type 2 have significant morbidity and require careful follow-up. Kidney Int 96:1389–1399

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