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首页> 外文期刊>American journal of medical genetics, Part A >Arthropathy, osteolysis, keloids, relapsing conjunctival pannus and gingival overgrowth: A variant of polyfibromatosis?
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Arthropathy, osteolysis, keloids, relapsing conjunctival pannus and gingival overgrowth: A variant of polyfibromatosis?

机译:关节炎,溶骨,瘢痕loid,结膜囊pan复发和牙龈过度生长:多发性纤维瘤病的变种?

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摘要

Polyfibromatosis is a rare fibrosing condition characterized by fibromatosis in different body areas and by keloid formation, and which can be associated with arthropathy and osteolysis. Familial occurrence has been described, but the cause remains unknown. Here, we describe a patient with characteristics of polyfibromatosis with arthropathy who had in addition severe conjunctival fibrosis, distinctive face, gingival overgrowth, and pigmented keloids. We discuss the resemblances and differences with polyfibromatosis and descriptions of other, similar patients. We conclude that at present it remains uncertain whether the patient has a variant of polyfibromatosis or a separate entity.
机译:多纤维瘤病是一种罕见的纤维化疾病,其特征在于不同身体部位的纤维瘤病和瘢痕loid形成,并且可能与关节病和溶骨有关。已经描述了家族性发生,但是原因仍然未知。在这里,我们描述了具有关节炎的多纤维瘤病特征的患者,该患者还患有严重的结膜纤维化,独特的面部,牙龈过度生长和色素性瘢痕loid。我们讨论了与多纤维瘤病的相似之处和差异,以及其他相似患者的描述。我们得出的结论是,目前尚不确定患者是否患有多纤维瘤病变体或单独的实体。

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