[A case of neonatal hereditary spherocytosis characterized by hydrops fetalis]

Zhonghua Er Ke Za Zhi. 2020 May 2;58(5):418-420. doi: 10.3760/cma.j.cn112140-20200113-00030.
[Article in Chinese]

Abstract

1例以宫内胎儿水肿为特征的患儿,新生儿期表现为间接胆红素增高为主的重度高胆红素血症、网织红细胞比例增高、重度贫血、肝脾肿大。基因测序结果显示存在SPTB基因移码变异,为c.5165_c.5166delTT,为新发变异,确诊为遗传性球形红细胞增多症。以非免疫性胎儿水肿为特征的遗传性球形红细胞增多症少见,对于临床高度怀疑而常规辅助检查不支持的新生儿遗传性球形红细胞增多症,基因检测可协助确诊。.

Publication types

  • Case Reports

MeSH terms

  • Humans
  • Hydrops Fetalis*
  • Infant, Newborn
  • Spherocytosis, Hereditary*