Bravo-Piris J, Villaron L G, Martinez C, Garcia-Perez A
Dermatologica. 1976;152(3):168-76. doi: 10.1159/000251244.
Two cases with Papillon-Lefèvre Syndrome (PLS) are reported. They are two brothers belonging to a family which there is strong consanguinity. An autosomal recessive pattern of inheritance is suggested. Some pathological findings as congenital bronchiectasis observed in one of the patients as well as the PLS features are discussed and considered to be fortuitous defects. These observations are compared with those described in the literature.
报告了两例帕皮永-勒费夫尔综合征(PLS)患者。他们是来自一个有很强血缘关系家庭的两兄弟。提示为常染色体隐性遗传模式。讨论了其中一名患者观察到的一些病理结果,如先天性支气管扩张以及PLS特征,并认为是偶然缺陷。将这些观察结果与文献中描述的结果进行了比较。