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Updated: Jun 25, 2026

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
Nijmegen breakage syndrome associated with porokeratosis
Elizabeth K Wolf1, Tor A Shwayder
1Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Abstract:
Nijmegen breakage syndrome (NBS) is a rare DNA repair disorder caused by mutations in the NBS-1 gene (8q21). Patients with this autosomal recessive condition have characteristic facial features, microcephaly present at birth, immunodeficiency, predisposition to malignancy, ionizing radiation hypersensitivity, and growth retardation. We report a 12-year-old boy with NBS associated with porokeratosis; to our knowledge this association has not previously been reported.
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