Horton W A, Rimoin D L, Lachman R S, Skovby F, Hollister D W, Spranger J, Scott C I, Hall J G
J Pediatr. 1978 Oct;93(4):609-13. doi: 10.1016/s0022-3476(78)80896-8.
To determine the relationship between so-called "diastrophic variant" and diastrophic dysplasia, four patients considered to have the variant condition were studied in detail and compared to 67 patients (including 17 sets of affected sibs) considered to have classical diastrophic dysplasia. Analysis of the combined clinical, radiographic, histologic, and genetic data indicates that there is wide variability in the phenotypic expression of diastrophic dysplasia, even within sibships, and that those individuals previously labeled as having "diastrophic variant" appear to have mild diastrophic dysplasia.
为了确定所谓的“畸形性变体”与畸形性发育不良之间的关系,对4例被认为患有该变体疾病的患者进行了详细研究,并与67例(包括17组患病同胞)被认为患有典型畸形性发育不良的患者进行了比较。对综合临床、影像学、组织学和遗传学数据的分析表明,即使在同胞之间,畸形性发育不良的表型表达也存在很大差异,并且那些先前被标记为患有“畸形性变体”的个体似乎患有轻度畸形性发育不良。