Cobalamin C Deficiency: An Uncommon Cause of Hemolytic Uremic Syndrome-Reference-Cited by-同舟云学术

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Cobalamin C Deficiency: An Uncommon Cause of Hemolytic Uremic Syndrome

Published:2024-04-05 Issue:7 Volume:61 Page:691-693
ISSN:0019-6061
Container-title:Indian Pediatrics
language:en
Short-container-title:Indian Pediatr

Author:

Singh Kanika,Pandey Mukul,Uttam Rajiv,Sethi Sidharth Kumar

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s13312-024-3238-5.pdf

Reference7 articles.

1. Genest DS, Patriquin CJ, Licht C, et al. Renal thrombotic microangiopathy: A review. Am J Kidney Dis.2023;81:591–605.

2. Loirat C, Fakhouri F, Ariceta G, et al. HUS International. An international consensus approach to the management of atypical haemolytic uremic syndrome in children. Pediatr Nephrol.2016;31:15–39.

3. Huemer M, Diodato D, Schwahn B, et al. Guidelines for Diagnosis and Management of the Cobalamin-related Remethylation Disorders CblC, CblD, CblE, CblF, CblG, CblJ and MTHFR deficiency. J Inherited Metab Dis.2017; 40:21–48.

4. Huemer M, Diodato D, Martinelli D, et al. Phenotype, treatment practice and outcome in the cobalamin-dependent remethylation disorders and MTHFR deficiency: Data from the E-HOD registry. J Inherit Metab Dis.2019;42:333–52.

5. Kaur R, Attri SV, Saini AG, et al. A high frequency and geographical distribution of MMACHCR132* mutation in children with cobalamin C defect. Amino acids.2021;53: 253–64.

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