Literature DB >> 28610805

Cobalamin disorder CblC presenting with hemolytic uremic syndrome and pulmonary hypertension.

Zuriñe Martínez de Compañón1, Miriam Poblet-Puig2, Griselda Vallès2, Mireia Del Toro3, Ramón Vilalta4, Antonio Moreno5, Joan Balcells2.   

Abstract

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Year:  2017        PMID： 28610805     DOI： 10.1016/j.nefro.2017.03.019

Source DB:  PubMed          Journal:  Nefrologia (Engl Ed)        ISSN： 2013-2514


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  4 in total

1.  Hemolytic Uremic Syndrome Due to Methylmalonic Acidemia and Homocystinuria in an Infant: A Case Report and Literature Review.

Authors:  Vasiliki Karava; Antonia Kondou; John Dotis; Georgia Sotiriou; Spyridon Gerou; Helen Michelakakis; Euthymia Vargiami; Marina Economou; Dimitrios Zafeiriou; Nikoleta Printza
Journal:  Children (Basel)       Date:  2021-02-05

2.  Case Report: A Rare Case of Thrombotic Microangiopathy Induced by Remethylation Disorders.

Authors:  Lu Pang; Jian Chen; Haiyan Yu; Haiming Huang; Bo Jin; Xin Wang; Haixia Li
Journal:  Front Med (Lausanne)       Date:  2022-03-02

3.  Clinical, phenotypic and genetic landscape of case reports with genetically proven inherited disorders of vitamin B12 metabolism: A meta-analysis.

Authors:  Arnaud Wiedemann; Abderrahim Oussalah; Nathalie Lamireau; Maurane Théron; Melissa Julien; Jean-Philippe Mergnac; Baptiste Augay; Pauline Deniaud; Tom Alix; Marine Frayssinoux; François Feillet; Jean-Louis Guéant
Journal:  Cell Rep Med       Date:  2022-06-27

4.  Adult-onset hypoxaemia, diffuse lung lesions, and pulmonary hypertension in cobalamin C defect: a case report.

Authors:  Qin-Hua Zhao; Wen-Hui Wu; Li-Jun Fu; Lan Wang
Journal:  Eur Heart J Case Rep       Date:  2021-06-30
  4 in total

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