Ciana Giovanni, Trappan Antonella, Bembi Bruno, Benettoni Alessandra, Maso Giampaolo, Zennaro Floriana, Ruf Nico, Schnabel Dirk, Rutsch Frank
S.C. di Neonatologia e Terapia Intensiva Neonatale, Istituto per l'Infanzia Burlo Garofolo, Via dell'Istria 65/1-34100, Trieste, Italy.
Eur J Pediatr. 2006 Apr;165(4):258-63. doi: 10.1007/s00431-005-0035-6. Epub 2005 Nov 29.
In generalized arterial calcification of infancy (OMIM no. 208000), calcification of the media and proliferation of the intima lead to arterial stenoses. Most affected patients present with untreatable arterial hypertension and die within the first months of life. The disease has recently been linked to mutations in ENPP1. We report two siblings with prolonged survival, both of whom carry the compound heterozygous ENPP1 mutations c.913C>A and c.1164+2T>A. In both siblings, spontaneous regression of arterial calcifications occurred, and antihypertensive treatment could be tapered off gradually. In some patients, the natural course of GACI may be more favourable than previously assumed.
在婴儿期全身性动脉钙化(OMIM编号208000)中,中膜钙化和内膜增生会导致动脉狭窄。大多数受影响的患者会出现无法治疗的动脉高血压,并在出生后的头几个月内死亡。该疾病最近被发现与ENPP1基因突变有关。我们报告了两名存活时间延长的兄弟姐妹,他们都携带复合杂合的ENPP1基因突变c.913C>A和c.1164+2T>A。在这两名兄弟姐妹中,动脉钙化均自发消退,并且抗高血压治疗可以逐渐减少剂量。在一些患者中,婴儿期全身性动脉钙化的自然病程可能比之前认为的更为有利。