El-Darouti Mohamed, Zayed Amira A, El-Kamah Ghada Y, Mostafa Mostafa I
Department of Dermatology, Cairo University, Cairo, Egypt.
Pediatr Dermatol. 2009 Jul-Aug;26(4):448-51. doi: 10.1111/j.1525-1470.2009.00951.x.
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.
木样结膜炎（MIM 217090）是一种罕见的常染色体隐性遗传性疾病。我们报告一例同时患有木样结膜炎和木样牙周炎并伴有I型纤溶酶原缺乏的病例。诊断基于临床和组织学检查结果，最重要的是，血清I型纤溶酶原水平降低。
