Journal Article

PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus

Hattori, Ai, Shiraishi, Yuichi, Chiba, Kenichi, Ogawa, Seishi, Usui, Takeshi, Tatsumi, Yasuaki, Kato, Koichi, Oe, Keishi, Sugihara, Takashi, Yoshida, Kenichi, Muramatsu, Hideki, Tanaka, Hiroko, Miyano, Satoru, Sueyoshi, Atsushi, Kojima, Seiji, Kanno, Hitoshi, Okuno, Yusuke, Wang, Xinan, Kita, Shinya, Kato, Ayako, Imashuku, Shinsaku

2016

Overview

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.

• Publisher: Springer Japan,Springer Nature B.V
• Subject: Anemia, Hemolytic, Congenital - diagnosis / Anemia, Hemolytic, Congenital - genetics / Anemia, Hemolytic, Congenital Nonspherocytic - diagnosis / Anemia, Hemolytic, Congenital Nonspherocytic - genetics / Asian Continental Ancestry Group / Case Report / Diabetes Mellitus - etiology / Family Health / Female / Hematology / Hemochromatosis - complications / Humans / Hydrops Fetalis - diagnosis / Ion Channels - genetics / Male / Medicine / Medicine & Public Health / Mutation / Oncology / Pedigree / Phosphatidylcholines