Literature DB >> 30187933

Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients.

Immacolata Andolfo1,2, Roberta Russo1,2, Barbara Eleni Rosato1,2, Francesco Manna1,2, Antonella Gambale1,2, Carlo Brugnara3, Achille Iolascon1,2.   

Abstract

Hereditary stomatocytoses (HSts) are a wide spectrum of hemolytic anemias in which the erythrocyte membrane cation permeability is increased. Dehydrated hereditary stomatocytosis is the most frequent among HSts. It is caused by missense mutations in PIEZO1 and KCNN4 genes. We described 123 patients enrolled in our Genetic Unit from 2013 to 2017. Overall HSt subjects exhibit macrocytic mild anemia. We found that PIEZO1 is the most frequent mutated gene within our families (47% of pedigrees). In 59.1% of cases the mutations localized in the nonpore protein domain, while in 40.9% of patients they localized in the central pore region. The genotype-phenotype correlation analysis on 29 PIEZO1-patients demonstrated that most of severely affected patients carried mutations in the pore domain, suggesting that the severity of this condition is related to the pore properties and intracellular domain that could be responsible of interactions with intracellular components. This is the first cohort study on a large set of hereditary stomatocytosis patients, stratified according to their causative gene useful for diagnosis, prognosis, and management of these patients.
© 2018 Wiley Periodicals, Inc.

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Year:  2018        PMID: 30187933     DOI: 10.1002/ajh.25276

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


  14 in total

1.  Gardos channelopathy: functional analysis of a novel KCNN4 variant.

Authors:  Elisa Fermo; David Monedero-Alonso; Polina Petkova-Kirova; Asya Makhro; Laurent Pérès; Guillaume Bouyer; Anna Paola Marcello; Filomena Longo; Giovanna Graziadei; Wilma Barcellini; Anna Bogdanova; Stephane Egee; Lars Kaestner; Paola Bianchi
Journal:  Blood Adv       Date:  2020-12-22

2.  Red cell membrane disorders: structure meets function.

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

3.  Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency.

Authors:  Paola Bianchi; Elisa Fermo; Bertil Glader; Hitoshi Kanno; Archana Agarwal; Wilma Barcellini; Stefan Eber; James D Hoyer; David J Kuter; Tabita Magalhães Maia; Maria Del Mar Mañu-Pereira; Theodosia A Kalfa; Serge Pissard; José-Carlos Segovia; Eduard van Beers; Patrick G Gallagher; David C Rees; Richard van Wijk
Journal:  Am J Hematol       Date:  2018-11-28       Impact factor: 10.047

4.  PIEZO1 gain-of-function mutations delay reticulocyte maturation in hereditary xerocytosis.

Authors:  Pedro L Moura; Bethan R Hawley; Johannes G G Dobbe; Geert J Streekstra; Minke A E Rab; Paola Bianchi; Richard van Wijk; Ashley M Toye; Timothy J Satchwell
Journal:  Haematologica       Date:  2019-10-17       Impact factor: 9.941

5.  Nobel prize in physiology or medicine 2021, receptors for temperature and touch: Implications for hematology.

Authors:  Immacolata Andolfo; Seth L Alper; Achille Iolascon
Journal:  Am J Hematol       Date:  2021-11-20       Impact factor: 13.265

Review 6.  A novel PIEZO1 mutation in a patient with dehydrated hereditary stomatocytosis: a case report and a brief review of literature.

Authors:  Daniele Zama; Giulia Giulietti; Edoardo Muratore; Immacolata Andolfo; Roberta Russo; Achille Iolascon; Andrea Pession
Journal:  Ital J Pediatr       Date:  2020-07-23       Impact factor: 2.638

7.  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

8.  CoDysAn: A Telemedicine Tool to Improve Awareness and Diagnosis for Patients With Congenital Dyserythropoietic Anemia.

Authors:  Cristian Tornador; Edgar Sánchez-Prados; Beatriz Cadenas; Roberta Russo; Veronica Venturi; Immacolata Andolfo; Ines Hernández-Rodriguez; Achille Iolascon; Mayka Sánchez
Journal:  Front Physiol       Date:  2019-09-13       Impact factor: 4.566

Review 9.  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

Review 10.  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

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