Moog U, Engelen J, Albrechts J, Hoorntje T, Hendrikse F, Schrander-Stumpel C
Department of Molecular Cell Biology and Genetics, University of Limburg, Maastricht, The Netherlands.
Clin Dysmorphol. 1996 Oct;5(4):279-88.
Alagille syndrome (arteriohepatic dysplasia, AHD) is a well defined genetic disorder with five major features: distinctive facies, cardiovascular anomalies, paucity of interlobular bile ducts (PILBD), ocular anomalies and minor skeletal malformations. Repeatedly, structural anomalies of 20p, in most cases a deletion, have been described in patients with Alagille syndrome. We report a three generation family with AHD presenting with typical facial dysmorphology, cardiac and ocular lesions but without clinical signs of liver manifestation. Two infants died from a complex cardiovascular malformation consisting of pulmonary valve atresia, hypoplasia of the pulmonary arteries and VSD. The diagnosis was not appreciated until ocular anomalies were found in the father and the distinctive facies became apparent in the daughter. Chromosome region 20p could not be interpreted precisely by high resolution banding. Using in situ hybridization a duplication 20p11.21-p11.23 was found segregating with the disorder in the family.
阿拉吉耶综合征(动脉肝发育不良,AHD)是一种明确的遗传性疾病,具有五个主要特征:特殊面容、心血管异常、小叶间胆管稀少(PILBD)、眼部异常和轻度骨骼畸形。反复有报道称,阿拉吉耶综合征患者存在20号染色体短臂的结构异常,大多数情况下为缺失。我们报告了一个三代家族患有AHD,表现出典型的面部畸形、心脏和眼部病变,但无肝脏表现的临床体征。两名婴儿死于复杂的心血管畸形,包括肺动脉瓣闭锁、肺动脉发育不全和室间隔缺损。直到在父亲身上发现眼部异常且女儿身上出现特殊面容后,才做出诊断。高分辨率显带无法精确解读20号染色体短臂区域。通过原位杂交发现,20p11.21-p11.23重复与该家族中的疾病共分离。