Literature DB >> 28971506

Hereditary stomatocytosis: An underdiagnosed condition.

Immacolata Andolfo1,2, Roberta Russo1,2, Antonella Gambale1,2, Achille Iolascon1,2.   

Abstract

Hereditary stomatocytoses are a wide class of hemolytic anemias characterized by alterations of ionic flux with increased cation permeability that results in inappropriate shrinkage or swelling of the erythrocytes, and water lost or gained osmotically. The last few years have been crucial for new acquisitions in this field in terms of identifying new causative genes and of studying their pathogenetic mechanisms. This review summarizes the main features of erythrocyte membrane transport diseases, dividing them into forms with either isolated erythroid phenotype (nonsyndromic) or extra-hematological manifestations (syndromic), and focusing particularly on the most recent advances regarding dehydrated forms of hereditary stomatocytosis and familial pseudohyperkalemia.
© 2017 Wiley Periodicals, Inc.

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Year:  2017        PMID: 28971506     DOI: 10.1002/ajh.24929

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  14 in total

1.  Red cell membrane disorders: structure meets function.

Authors:  Mary Risinger; Theodosia A Kalfa
Journal:  Blood       Date:  2020-09-10       Impact factor: 22.113

Review 2.  The Molecular Basis for Altered Cation Permeability in Hereditary Stomatocytic Human Red Blood Cells.

Authors:  Joanna F Flatt; Lesley J Bruce
Journal:  Front Physiol       Date:  2018-04-16       Impact factor: 4.566

3.  Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients.

Authors:  Véronique Picard; Corinne Guitton; Isabelle Thuret; Christian Rose; Laurence Bendelac; Kaldoun Ghazal; Patricia Aguilar-Martinez; Catherine Badens; Claire Barro; Claire Bénéteau; Claire Berger; Pascal Cathébras; Eric Deconinck; Jacques Delaunay; Jean-Marc Durand; Nadia Firah; Frédéric Galactéros; Bertrand Godeau; Xavier Jaïs; Jean-Pierre de Jaureguiberry; Camille Le Stradic; François Lifermann; Robert Maffre; Gilles Morin; Julien Perrin; Valérie Proulle; Marc Ruivard; Fabienne Toutain; Agnès Lahary; Loïc Garçon
Journal:  Haematologica       Date:  2019-01-17       Impact factor: 9.941

Review 4.  Genetics and Genomics Approaches for Diagnosis and Research Into Hereditary Anemias.

Authors:  Roberta Russo; Roberta Marra; Barbara Eleni Rosato; Achille Iolascon; Immacolata Andolfo
Journal:  Front Physiol       Date:  2020-12-22       Impact factor: 4.566

5.  Identification of a Novel Mutation of β-Spectrin in Hereditary Spherocytosis Using Whole Exome Sequencing.

Authors:  Dżamila M Bogusławska; Michał Skulski; Beata Machnicka; Stanisław Potoczek; Sebastian Kraszewski; Kazimierz Kuliczkowski; Aleksander F Sikorski
Journal:  Int J Mol Sci       Date:  2021-10-12       Impact factor: 5.923

6.  [Pathogenesis and diagnosis of hereditary stomatocytosis].

Authors:  J Q Li; B H Qian
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2020-06-14

Review 7.  Congenital Hemolytic Anemias: Is There a Role for the Immune System?

Authors:  Anna Zaninoni; Elisa Fermo; Cristina Vercellati; Anna Paola Marcello; Wilma Barcellini; Paola Bianchi
Journal:  Front Immunol       Date:  2020-06-23       Impact factor: 7.561

8.  Yoda1 and phosphatidylserine exposure in red cells from patients with sickle cell anaemia.

Authors:  R Wadud; A Hannemann; D C Rees; J N Brewin; J S Gibson
Journal:  Sci Rep       Date:  2020-11-18       Impact factor: 4.379

9.  Rare Anemias: Are Their Names Just Smoke and Mirrors?

Authors:  Greta Simionato; Richard van Wijk; Stephan Quint; Christian Wagner; Paola Bianchi; Lars Kaestner
Journal:  Front Physiol       Date:  2021-06-10       Impact factor: 4.566

10.  Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 Patients.

Authors:  Immacolata Andolfo; Stefania Martone; Barbara Eleni Rosato; Roberta Marra; Antonella Gambale; Gian Luca Forni; Valeria Pinto; Magnus Göransson; Vasiliki Papadopoulou; Mathilde Gavillet; Mohsen Elalfy; Antonella Panarelli; Giovanna Tomaiuolo; Achille Iolascon; Roberta Russo
Journal:  Genes (Basel)       Date:  2021-06-23       Impact factor: 4.096

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