| Literature DB >> 26971963 |
Shinsaku Imashuku1, Hideki Muramatsu2, Takashi Sugihara3, Yusuke Okuno2,4, Xinan Wang2, Kenichi Yoshida5, Ayako Kato6, Koichi Kato6, Yasuaki Tatsumi6, Ai Hattori7, Shinya Kita8, Keishi Oe8, Atsushi Sueyoshi8, Takeshi Usui9, Yuichi Shiraishi10, Kenichi Chiba10, Hiroko Tanaka11, Satoru Miyano10,11,12, Seishi Ogawa5, Seiji Kojima2, Hitoshi Kanno13.
Abstract
Hereditary xerocytosis (HX) or dehydrated hereditary stomatocytosis (DHS) [OMIM 194380], in which PIEZO1 gene mutation has recently been identified, is difficult to diagnose. We report here the discovery of a PIEZO1 gene mutation in a Japanese family (father, daughter, and son) who were previously diagnosed with hereditary high phosphatidylcholine hemolytic anemia (HPCHA). All of the affected family members had non-spherocytic hemolytic anemia associated with severe hemochromatosis-related diabetes mellitus. Although the causative correlation between HPCHA and PIEZO1-gene mutated HX/DHS remains to be clarified, our findings raise an important question as to whether any of the HPCHA cases previously diagnosed in Japan may have in fact been the form of hemolytic anemia known as HX/DHS with PIEZO1 gene mutation.Entities:
Keywords: Hemochromatosis; Hereditary high phosphatidylcholine hemolytic anemia; Macrocytic hemolytic anemia; PIEZO1 gene mutation; Stomatocytosis
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Year: 2016 PMID: 26971963 DOI: 10.1007/s12185-016-1970-x
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490