Department of Pediatrics, Seoul National University Children's Hospital, Seoul, Korea.
Department of Pediatrics, Seoul National University Children's Hospital, Seoul, Korea ; Research Center for Rare Diseases, Seoul National University Hospital, Seoul, Korea.
Clin Kidney J. 2012 Feb;5(1):56-8. doi: 10.1093/ndtplus/sfr153. Epub 2012 Jan 28.
Autosomal-recessive renal tubular dysgenesis (AR-RTD) is a rare disorder caused by a genetic defect in the renin-angiotensin system. Although AR-RTD has typically been known as a lethal disease due to refractory hypotension and renal failure immediately after birth, few cases have reported survival of the neonatal period. We report here an additional case of AR-RTD, who had novel ACE mutations and survived over 2 years and provide a review of the five previously reported surviving cases. In conclusion, AR-RTD is not a uniformly fatal disease, although factors affecting the survival remain unknown.
常染色体隐性遗传性肾小管发育不良(AR-RTD)是一种由肾素-血管紧张素系统遗传缺陷引起的罕见疾病。尽管 AR-RTD 通常由于出生后立即出现难治性低血压和肾衰竭而被认为是一种致命疾病,但很少有新生儿期存活的病例报告。我们在此报告另一个 AR-RTD 病例,该病例具有新的 ACE 突变并存活超过 2 年,并对以前报道的 5 例存活病例进行了回顾。总之,AR-RTD 并非一种普遍致命的疾病,尽管影响生存的因素尚不清楚。