期刊
PEDIATRIC DERMATOLOGY
卷 26, 期 4, 页码 448-451出版社
WILEY-BLACKWELL PUBLISHING, INC
DOI: 10.1111/j.1525-1470.2009.00951.x
关键词
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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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