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Correspondence comprehensive characterization of a brainstem aggregoma (light and heavy chain deposition disease).

Authors :
Becker, Aline P.
Osorio, Diana S.
Bell, Erica H.
Giglio, Pierre
Fleming, Jessica L.
Cottrell, Catherine E.
Mardis, Elaine R.
Miller, Katherine E.
Schieffer, Kathleen M.
Kelly, Benjamin J.
Makary, Mina S.
Slone, Wayne
Benson, Don
Leonard, Jeffrey
Kahwash, Samir B.
Boué, Daniel R.
Chakravarti, Arnab
Source :
Brain Pathology. Sep2023, Vol. 33 Issue 5, p1-5. 5p.
Publication Year :
2023

Abstract

(B) mRNA expression of select immunoglobulin chain genes (detected at highest abundance in LC-MS/MS data) in a cohort of 153 pediatric CNS lesions. (A) Most abundant proteins detected by LC-MS/MS analysis of the LHCDD - number of proteins compared with the total spectrum count. Our patient sample is highlighted in red. (C) Ingenuity pathway analysis pathway analysis showed elevated immune pathways with a positive Z score, confirming the findings from LC-MS/MS. Keywords: aggregoma; genomic profiling; immunoglobulin kappa-chains; light and heavy chain deposition disease; mass spectrometry EN aggregoma genomic profiling immunoglobulin kappa-chains light and heavy chain deposition disease mass spectrometry 1 5 5 09/01/23 20230901 NES 230901 Monoclonal immunoglobulin (Ig) deposition diseases are classified as heavy chain deposition disease (HCDD); light chain deposition diseases (LCDD); and light and heavy chain deposition disease (LHCDD) - deposits of both light [kappa ( ) and lambda ( )], and heavy [alpha ( ), delta ( ), epsilon ( ), gamma ( ), and mu ( )] Ig chains. [Extracted from the article]

Details

Language :
English
ISSN :
10156305
Volume :
33
Issue :
5
Database :
Academic Search Index
Journal :
Brain Pathology
Publication Type :
Academic Journal
Accession number :
171106109
Full Text :
https://doi.org/10.1111/bpa.13154