| Literature DB >> 19689523 |
Mohamed El-Darouti1, Amira A Zayed, Ghada Y El-Kamah, Mostafa I Mostafa.
Abstract
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.Entities:
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Year: 2009 PMID: 19689523 DOI: 10.1111/j.1525-1470.2009.00951.x
Source DB: PubMed Journal: Pediatr Dermatol ISSN: 0736-8046 Impact factor: 1.588