Journal
PEDIATRIC DERMATOLOGY
Volume 26, Issue 4, Pages 448-451Publisher
WILEY-BLACKWELL PUBLISHING, INC
DOI: 10.1111/j.1525-1470.2009.00951.x
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Ligneous conjunctivitis (MIM 217090) is a rare autosomal recessive hereditary disorder. We report a case with both ligneous conjunctivitis and ligneous periodontitis in association with plasminogen type I deficiency. Diagnosis was based on the clinical and histological findings and most importantly, decreased serum level of plasminogen type I.
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