匐行性穿通性弹力纤维病。一家系报告。

Dermatologica. 1983;166(1):32-7.

Two brothers with typical, symmetrical lesions of elastosis perforans serpiginosa are presented. Familial occurrence has been reported only once. In neither family was the disease associated with heritable disorders of the connective tissue. The pedigree analysis suggests an autosomal-recessive pattern of inheritance.

本文报告了两例患有典型对称性匐行性穿通性弹力纤维病损的兄弟。家族性发病仅曾有过一次报道。在这两个家族中，该病均与结缔组织的遗传性疾病无关。系谱分析提示为常染色体隐性遗传模式。