Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy
Date
2014Author
Winkelmann, Juliane
Levy-Lahad, Ephrat
King, Mary-Claire
Anikster, Yair
Sener, Elif F.
Schormair, Barbara
Zeligson, Sharon
Marek-Yagel, Dina
Strom, Tim M.
Shohat, Mordechai
Singer, Amihood
Rubinow, Alan
Pras, Elon
Tekin, Mustafa
Padeh, Shai
Zlotogorski, Abraham
Berkun, Yackov
Press, Joseph J.
Mukamel, Masha
Voth, Isabel
Hashkes, Philip J.
Harel, Liora
Hoffer, Vered
Ling, Eduard
Pierce, Sarah B.
Segel, Reeval
Walsh, Tom
Barash, Judith
Yalcinkaya, Fatos
Lee, Ming K.
Klevit, Rachel E.
Renbaum, Paul
Weinberg-Shukron, Ariella
Elkan, Paulina Navon
Kasapcopur, Ozgur
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Show full item recordAbstract
BackgroundPolyarteritis nodosa is a systemic necrotizing vasculitis with a pathogenesis that is poorly understood. We identified six families with multiple cases of systemic and cutaneous polyarteritis nodosa, consistent with autosomal recessive inheritance. In most cases, onset of the disease occurred during childhood.
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