作为一种罕见的遗传性疾病,乙烯基塑胺血症:在一个中心报告了四例病例

Zülal İstemihan1, Ziya İmanov1, Bilger Çavuş1

  • 1Division of Gastroenterohepatology, Department of Internal Medicine, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Türkiye.

Proceedings (Baylor University. Medical Center)
|February 24, 2025
PubMed
概括

乙烯基塑血症是一种罕见的铁性疾病,往往表现为模糊的症状. 查至关重要,特别是在血缘关系婚姻的家庭中,以早期发现这种情况.