C1q Nephropathy in a Patient of Neurofibromatosis Type 1: A Rare Case Report

C1q nephropathy is a rare glomerular disease defined by the presence of characteristic mesangial dominant or codominant C1q deposition on immunofluorescence microscopy. Neurofibromatosis type 1 (NF-1) is an autosomal dominant syndrome caused by a mutation of a gene located on chromosomal segment 17q...

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Detalles Bibliográficos
Autores principales: Varyani, U. T., Shah, N. M., Shah, P. R., Kute, V. B., Balwani, M. R., Trivedi, H. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6440327/
https://www.ncbi.nlm.nih.gov/pubmed/30983754
http://dx.doi.org/10.4103/ijn.IJN_353_17
Descripción
Sumario:C1q nephropathy is a rare glomerular disease defined by the presence of characteristic mesangial dominant or codominant C1q deposition on immunofluorescence microscopy. Neurofibromatosis type 1 (NF-1) is an autosomal dominant syndrome caused by a mutation of a gene located on chromosomal segment 17q11.2. Nephrotic syndrome has rarely been reported in patients of NF-1, and the relation of NF-1 with nephrotic syndrome is unclear. Here, we present a rare case of C1q nephropathy in a patient of NF-1.

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