| Autor: |
Varyani, U. T., Shah, N. M., Shah, P. R., Kute, V. B., Balwani, M. R., Trivedi, H. L. |
| Předmět: |
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| Zdroj: |
Indian Journal of Nephrology; Mar/Apr2019, Vol. 29 Issue 2, p125-127, 3p |
| Abstrakt: |
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. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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