Bamshad M, Bohnsack J F, Jorde L B, Carey J C
Department of Pediatrics, University of Utah Health Sciences Center, Salt Lake City 84132-1001, USA.
Am J Med Genet. 1996 Nov 11;65(4):282-5. doi: 10.1002/(SICI)1096-8628(19961111)65:4<282::AID-AJMG7>3.0.CO;2-R.
We describe the clinical findings of 15 individuals in a large kindred affected with distal arthrogryposis type 1A (DA1A). The most consistent findings among individuals were overlapping fingers at birth, abnormal digital flexion creases, and foot deformities, including talipes equinovarus and vertical talus. There was marked intrafamilial variation in the expression of DA1A. Linkage mapping of the locus for DA1A suggests that the use of strict diagnostic criteria excludes unaffected individuals rigorously, but can produce incomplete ascertainment of affected individuals. In the context of an affected family, the range of phenotypes consistent with a diagnosis of DA1A needs to be expanded.
我们描述了一个患有1A型远端关节挛缩症(DA1A)的大家族中15名个体的临床发现。个体中最一致的发现是出生时手指重叠、异常的指屈纹以及足部畸形,包括马蹄内翻足和垂直距骨。DA1A的表达在家族内部存在显著差异。DA1A基因座的连锁图谱表明,使用严格的诊断标准能严格排除未患病个体,但可能导致对患病个体的不完全确诊。在一个患病家族的背景下,与DA1A诊断相符的表型范围需要扩大。