Systemic lupus erythematosus occurring in a patient with Niemann-Pick type B disease.

MURGIA, GIUSEPPE;FIRINU, DAVIDE;MELEDDU, RITA;LORRAI, MARIA MADDALENA;MANCONI, PAOLO EMILIO;DEL GIACCO, STEFANO
2015-01-01

Abstract

Niemann-Pick disease is an inherited lipid storage disorder caused by the deficiency of acid sphingomyelinase, which results in accumulation of sphingomyelin within cells of several organs and consequent tissue damage. The broad clinical spectrum of this disorder may overlap with that of systemic lupus erythematosus, hindering differential diagnosis. Herein, we report the case of a patient affected by Niemann-Pick type B disease intertwined with clinical and serological features of systemic lupus erythematosus. Two novel mutations in the SMPD1 gene were found in compound heterozygosity: p.A36V and IVS2 + 8 T > G.
2015
AUTOIMMUNITY, FEVER, LYSOSOMAL STORAGE DISORDER, NIEMANN-PICK, NIEMANN-PICK TYPE B DISEASE, SMPD1 GENE, SYSTEMIC LUPUS ERYTHEMATOSUS
Files in This Item:
File Size Format  
Lupus-2015-Murgia-1332-4.pdf

Solo gestori archivio

Type: versione post-print
Size 70.94 kB
Format Adobe PDF
70.94 kB Adobe PDF & nbsp; View / Open   Request a copy

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Questionnaire and social

Share on:
Impostazioni cookie