Bakaeen G, Scully C
Faculty of Dentistry, University of Jordan, Amman.
J Oral Pathol Med. 1991 Oct;20(9):457-9. doi: 10.1111/j.1600-0714.1991.tb00438.x.
Hereditary gingival fibromatosis is frequently an isolated condition of little consequence apart from a cosmetic problem and occasional associations with hypertrichosis and/or epilepsy. There are, however, several uncommon or rare eponymous syndromes described in which gingival fibromatosis can be a feature: these include the Zimmermann-Laband, Murray-Puretic-Drescher, Rutherfurd, Cowden and Cross syndromes. This paper describes two siblings with features of the rare Zimmermann-Laband syndrome and discusses the major aspects of this and other eponymous syndromes that may be associated with hereditary gingival fibromatosis.
遗传性牙龈纤维瘤病通常是一种孤立的病症，除了美容问题以及偶尔与多毛症和/或癫痫相关外，几乎没有其他影响。然而，有几种罕见的以人名命名的综合征，其中牙龈纤维瘤病可能是其特征之一：这些包括齐默尔曼 - 拉班德综合征、默里 - 普雷蒂克 - 德雷舍尔综合征、拉瑟福德综合征、考登综合征和克罗斯综合征。本文描述了两名具有罕见的齐默尔曼 - 拉班德综合征特征的兄弟姐妹，并讨论了这种综合征以及其他可能与遗传性牙龈纤维瘤病相关的以人名命名的综合征的主要方面。
