SIADH in a patient with sensory ataxic neuropathy with anti-disialosyl antibodies (CANOMAD)

Gabriella Silvestri, Raffaele Iorio, Fioravante Capone, Elisabetta Iannaccone, Anna Modoni, Pietro Attilio Tonali, Hugh John Willison

Risultato della ricerca: Contributo in rivistaArticolo in rivista

7 Citazioni (Scopus)

Abstract

CANOMAD (chronic ataxic neuropathy, opthalmoplegia, IgM paraprotein, cold agglutinins and disialosyl antibodies) is a rare variant of IgM paraproteinaemic neuropathy in which the paraprotein fraction contains antibodies against specific disialylated gangliosides, including GD1B, GD3, GT1B and GQ1B [1]. This disorder has so far not been reported in association with the syndrome of inappropriate secretion of antidiuretic hormone (SIADH). Here we describe a patient who developed SIADH during the first relapse of CANOMAD
Lingua originaleEnglish
pagine (da-a)1177-1179
Numero di pagine3
RivistaJournal of Neurology
Stato di pubblicazionePubblicato - 2009

Keywords

  • CANOMAD

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