Case Report: Membranous Nephropathy Secondary to Cobalamin C Disease

BACKGROUND: Mutation of MMACHC causes inherited cobalamin C disease with methylmalonic academia (MMA) and homocysteinemia. Renal complications may also be present in patients with this deficiency. However, membranous nephropathy secondary to cobalamin C disease has not been reported to date. CASE PR...

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Detalles Bibliográficos
Autores principales: Wang, Qiang, Wang, Qi, Gao, Yanxia, Tang, Chenquan, Gao, Zhaoli, Hu, Zhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8814342/
https://www.ncbi.nlm.nih.gov/pubmed/35127762
http://dx.doi.org/10.3389/fmed.2021.807017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8814342/
https://www.ncbi.nlm.nih.gov/pubmed/35127762
http://dx.doi.org/10.3389/fmed.2021.807017

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