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Incomplete Penetrance of the NOD2 E383K Substitution Among Members of a Pediatric Granulomatous Arthritis Pedigree

Journal

ARTHRITIS AND RHEUMATISM
Volume 60, Issue 6, Pages 1804-1806

Publisher

WILEY
DOI: 10.1002/art.24532

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Funding

  1. NIH [R01-EY-013139]

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Pediatric granulomatous arthritis (PGA) has been associated with 12 different substitutions in the NOD2 gene thus far. We report a case of PGA in a 6-year-old girl with the NOD2 E383K gene substitution. Genotype analysis of the patient's family members revealed that her affected paternal aunt, as well as her asymptomatic father and 3 younger siblings, were heterozygous for the E383K substitution. The patient's mother did not have a NOD2 mutation. This is the first report of a pedigree in which 4 asymptomatic members carry the E383K substitution in NOD2, as well as the first observation of an asymptomatic carrier state for any of the NOD2 Blau mutations.

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