André M, Vigneron J, Didier F
J Pediatr. 1981 May;98(5):747-52. doi: 10.1016/s0022-3476(81)80835-9.
Four boys of the same family (three first cousins and their uncle) had the same syndrome of multiple malformations. They had hypertelorism, antimongolian slant of the palpebral fissures, low-set ears, and Pierre Robin syndrome. The ossification of the skull vault was defective, with broad sutures and fontanelles. The ribs were sinuous, the clavicles were long, thin, and sloping, and the vertebrae were flattened. There were abnormal bowing with hyperostosis of the long bones, faulty ossification of the bones of hand and feet, and "fanned-out" toes. The disorder was lethal within a few weeks. The karyotype was normal. The mothers of affected boys had a mild form of the same abnormal facies. Transmission of this disorder appears to be linked to the X chromosome.
同一家庭的四个男孩(三个堂兄弟及其叔叔)患有相同的多发畸形综合征。他们有眼距增宽、睑裂反蒙古样倾斜、低位耳以及皮埃尔·罗宾综合征。颅顶骨化缺陷,缝和囟门宽阔。肋骨弯曲,锁骨长、细且倾斜,椎骨扁平。长骨有异常弯曲并伴有骨质增生,手足骨骼骨化不良,脚趾呈“扇形散开”。这种病症在几周内致命。核型正常。患病男孩的母亲有该异常面容的轻度表现形式。这种病症的遗传似乎与X染色体有关。