Miny P, Lenz W
Am J Med Genet. 1985 Jun;21(2):317-24. doi: 10.1002/ajmg.1320210214.
We report on two sibs born to consanguineous parents with clinical and radiological features closely resembling those previously described by Insley and Astley [1974]. This observation provides further evidence for a distinct autosomal recessive condition with the facial appearance of Marshall syndrome, deafness, and skeletal dysplasia.
我们报告了一对近亲结婚父母所生的同胞,其临床和放射学特征与Insley和Astley [1974] 先前描述的特征极为相似。这一观察结果为一种具有马歇尔综合征面部外观、耳聋和骨骼发育异常的独特常染色体隐性疾病提供了进一步的证据。