Shohat M, Rimoin D L, Gruber H E, Lachman R S
Medical Genetics and Pediatrics, Beilenson Medical Center, Petah Tikva, Israel.
Pediatr Radiol. 1991;21(6):421-7. doi: 10.1007/BF02026677.
Clinical, radiographic and morphologic analysis of nineteen cases of perinatal (lethal) hypophosphatasia was performed. Three families each had two affected offspring. All of the patients had lethal short limb dwarfism with very soft calvaria. Other clinical findings included polyhydramnios, blue sclerae and spurs in the mid-portion of the forearms and lower legs. Considerable variability was found in the skeletal radiographs. In addition to the well known radiographic features such as generalized decrease in the size of ossified bones with some bones not ossified at all, other changes observed included: 1) marked variability in the amount of bone ossification; 2) variability between patients as to which bones were most severely affected; 3) unusually dense, round, flattened, butterfly shaped; and sagittally clefted vertebral bodies; 4) variability in femoral shape including "chromosome" like, "campomelic" like, and shortening with or without metaphyseal cupping or irregularities; 5) osteochondral projections (Bowdler spurs) of the midshaft of the fibula and ulna. Recognition of the marked clinical and radiographic variability in this autosomal recessive lethal skeletal dysplasia is important for accurate genetic counseling and prenatal diagnosis.
对19例围产期(致死性)低磷酸酯酶症患者进行了临床、影像学和形态学分析。三个家庭各有两名患病后代。所有患者均患有致死性短肢侏儒症,颅骨非常柔软。其他临床发现包括羊水过多、蓝色巩膜以及前臂和小腿中部的骨刺。骨骼X光片显示出相当大的变异性。除了众所周知的影像学特征,如骨化骨大小普遍减小,有些骨头根本未骨化外,还观察到其他变化:1)骨化程度差异显著;2)不同患者中受影响最严重的骨头存在差异;3)椎体异常致密、圆形、扁平、蝴蝶形以及矢状裂;4)股骨形状各异,包括“染色体”样、“弯肢”样,以及伴有或不伴有干骺端杯口状或不规则的缩短;5)腓骨和尺骨中轴的骨软骨突出(鲍德勒骨刺)。认识到这种常染色体隐性致死性骨骼发育不良在临床和影像学上的显著变异性,对于准确的遗传咨询和产前诊断很重要。