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Case Reports in Hematology
Volume 2017 (2017), Article ID 2769570, 8 pages
https://doi.org/10.1155/2017/2769570
Case Report

Hereditary Xerocytosis due to Mutations in PIEZO1 Gene Associated with Heterozygous Pyruvate Kinase Deficiency and Beta-Thalassemia Trait in Two Unrelated Families

1U.O.C. Oncoematologia, U.O.S. Fisiopatologia delle Anemie, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milano, Italy
2Department of Clinical Chemistry and Haematology, University Medical Center Utrecht, Utrecht, Netherlands
3U.O.C. Pronto Soccorso, Pediatria Ambulatoriale e DH/MAC, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milano, Italy
4U.O.S.D. Genetica Medica, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milano, Italy
5Universita degli Studi di Milano, Milano, Italy

Correspondence should be addressed to Elisa Fermo; ti.oohay@omrefasile

Received 14 October 2016; Accepted 15 February 2017; Published 6 March 2017

Academic Editor: Ramon Tiu

Copyright © 2017 Elisa Fermo et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Elisa Fermo, Cristina Vercellati, Anna Paola Marcello, et al., “Hereditary Xerocytosis due to Mutations in PIEZO1 Gene Associated with Heterozygous Pyruvate Kinase Deficiency and Beta-Thalassemia Trait in Two Unrelated Families,” Case Reports in Hematology, vol. 2017, Article ID 2769570, 8 pages, 2017. doi:10.1155/2017/2769570