Congenital Analbuminemia in a Korean Male Diagnosed with Single Nucleotide Polymorphism in the ALB Gene: The First Case Reported in Korea
Sign Up to like & getrecommendations! Published in 2019 at "Yonsei Medical Journal"
DOI: 10.3349/ymj.2019.60.7.700
Abstract: Congenital analbuminemia (CAA) is an autosomal recessive disease characterized by extremely low serum levels of albumin. CAA is caused by various homozygous or heterozygous mutations of the ALB gene. Patients often exhibit no clinical symptoms,… read more here.
Keywords: congenital analbuminemia; reported korea; case; caa ... See more keywords
Eccrine Porocarcinoma: A Multicenter Retrospective Study with Review of the Literatures Reported in Korea
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DOI: 10.5021/ad.2020.32.3.223
Abstract: Background Eccrine porocarcinoma (EPC) is a rare malignant cutaneous adnexal tumor. Other than several scattered case reports, no comprehensive review on EPC has been conducted in Korea. Objective To clinicopathologically review all EPC cases from… read more here.
Keywords: reported korea; eccrine porocarcinoma; metastasis; review ... See more keywords