MacDermot K D, Roth S C, Hall C, Winter R M
Kennedy Galton Centre, Harperbury Hospital, London.
J Med Genet. 1987 Oct;24(10):602-8. doi: 10.1136/jmg.24.10.602.
A family is presented with short stature, femoral epiphyseal dysplasia, mild vertebral changes, and sensorineural deafness inherited as an autosomal dominant trait. Myopia and retinal detachment presenting in adult life were also present in some affected members. We suggest that this disorder may be a distinct entity within the spondyloepiphyseal dysplasia group of disorders.
一个家族呈现出身材矮小、股骨骨骺发育异常、轻度脊柱改变以及作为常染色体显性性状遗传的感音神经性耳聋。一些患病成员在成年期还出现近视和视网膜脱离。我们认为这种病症可能是脊椎骨骺发育异常疾病组中的一种独特病症。