Dermatologic Features of ADA2 Deficiency in Cutaneous Polyarteritis Nodosa




Tania M. Gonzalez Santiago, Andrey Zavialov, Janna Saarela, Mikko Seppanen, Ann M. Reed, Roshini S. Abraham, Lawrence E. Gibson

PublisherAmer Medical Assoc

2015

JAMA Dermatology

JAMA DERMATOLOGY

Jama Dermatol

151

11

1230

1234

5

2168-6068

DOIhttps://doi.org/10.1001/jamadermatol.2015.1635



CONCLUSIONS AND RELEVANCE These findings suggest a genetic cause of cPAN in some patients. Therefore, DADA2 should be considered in patients with cPAN, specifically in those whose conditions are diagnosed at an early age, regardless of their ethnicity, presence or absence of systemic symptoms, or a family history of the disease.




Last updated on 2024-26-11 at 20:23