Sánchez-Corona J, García-Cruz D, González-Angulo A, Alvarez-Arratia M C, Rodríguez R M, Cantú J M
Hum Genet. 1985;69(3):243-5. doi: 10.1007/BF00293033.
Two brothers and their sister aged 8, 13, and 7 years were found to have unusual facies (gross, rough and abundant hair, wide forehead, mild palpebral ptosis, small nose, anteverted nostrils, thick lips, and down-slanting corners of the mouth), dysarthria, delayed psychomotor development, scoliosis, feet deformities, and limb and gait ataxia. The characteristic clinical picture in the three sibs, once compared with other ataxic syndromes, allowed one to conclude that this could correspond to a distinct entity probably inherited as an autosomal recessive disorder.
发现两名兄弟及其8岁、13岁和7岁的妹妹有异常面容(面容粗糙、毛发浓密、额头宽阔、轻度上睑下垂、鼻子小、鼻孔前倾、嘴唇厚、嘴角向下倾斜)、构音障碍、精神运动发育迟缓、脊柱侧弯、足部畸形以及肢体和步态共济失调。这三名同胞的特征性临床表现一旦与其他共济失调综合征进行比较,就可以得出结论,这可能对应于一种独特的疾病实体,可能以常染色体隐性疾病的方式遗传。