Schmidt H, Ullrich K, von Lengerke H J, Kleine M, Brämswig J
Pediatr Radiol. 1987;17(5):409-14. doi: 10.1007/BF02396619.
The development of radiological changes in two patients with mucopolysaccharidosis (MPS) Type I H/S is described. Radiological findings reveal enlargement of the sella in one patient, impression of the basilar skull in the other patient. Sclerosis and thickening of the base of skull was observed in both patients. The mandibular necks were short with striking flattening of the superior surfaces of the condyles, when the patients reached adult age. At the age of 12, hypertelorism and spaced teeth were already present in both patients. In addition, they showed early costal, clavicular and scapular changes, irregularities of the acromial joints and acetabulae, hypoplasia of the inferior portion of the iliac bones and flared iliac wings. The flat femurs had short metaphyses and were held in valgus position. Development of dentigerous cysts as well as mandibular changes seem to be rather specific for this variant of alpha-L-iduronidase deficiency. In contrast to the classical form of MPS I, skeletal changes of the spine and hands are minimal.
本文描述了两名黏多糖贮积症 I H/S 型患者的放射学变化发展情况。放射学检查结果显示,一名患者蝶鞍增大,另一名患者颅底受压。两名患者均观察到颅底硬化和增厚。当患者成年时,下颌颈短,髁突上表面明显扁平。12岁时,两名患者均已出现眼距增宽和牙齿间隙增大。此外,他们还表现出早期的肋骨、锁骨和肩胛骨变化,肩锁关节和髋臼不规则,髂骨下部发育不全以及髂骨翼增宽。扁平的股骨干骺端短,并呈外翻位。牙源性囊肿的发生以及下颌骨变化似乎是这种α-L-艾杜糖醛酸酶缺乏变体的相当特异性表现。与经典的黏多糖贮积症 I 型相比,脊柱和手部的骨骼变化最小。