학술논문

Legg-Perthes disease in three siblings, two heterozygous and one homozygous for the factor V Leiden mutation.
Document Type
Academic Journal
Source
Journal of Pediatrics (J PEDIATR), 1998 May; 132(5): 885-888. (4p)
Subject
Language
English
ISSN
0022-3476
Abstract
A family is described with three-generation transmission of factor V Leiden (a thrombophilic mutation that causes resistance to activated protein C). Legg-Perthes disease developed in three siblings in this family. The male proband and his sister were heterozygous for the mutation and had unilateral hip disease at age 2 years. The brother, who had bilateral hip disease, was homozygous. This novel family provides compelling evidence for the pathoetiologic role of familial thrombophilia in Legg-Perthes disease.