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Hemoglobin
international journal for hemoglobin research
Volume 32, 2008 - Issue 3
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Original Article

Hb Agrinio [α29(B10)Leu→Pro (α2)] in Combination with – –MED I Results in a Severe Form of Hb H Disease

Xenia Felekis The Cyprus Institute of Neurology and Genetics, NicosiaCyprus
,
Marios Phylactides The Cyprus Institute of Neurology and Genetics, NicosiaCyprusCorrespondence[email protected]
,
Anthi Drousiotou The Cyprus Institute of Neurology and Genetics, NicosiaCyprus
,
Sotiroulla Christou Cyprus Thalassaemia Centre, Archbishop Makarios III Hospital, NicosiaCyprus
,
Andreani Kyrri Cyprus Thalassaemia Centre, Archbishop Makarios III Hospital, NicosiaCyprus
,
Kyriakos Kyriakou The Cyprus Institute of Neurology and Genetics, NicosiaCyprus
,
Eleni Kalogerou Cyprus Thalassaemia Centre, Archbishop Makarios III Hospital, NicosiaCyprus
,
George Christopoulos The Cyprus Institute of Neurology and Genetics, NicosiaCyprus
&
Marina Kleanthous The Cyprus Institute of Neurology and Genetics, NicosiaCyprus
 show all
Pages 237-246 | Received 05 Jul 2007, Accepted 02 Aug 2007, Published online: 07 Jul 2009

Citations (13)

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Marija Dimishkovska, Maja Kuzmanovska, Svetlana Kocheva, Kata Martinova, Oliver Karanfilski, Zlate Stojanoski & Dijana Plaseska-Karanfilska. (2017) First Cases of Hb Agrinio Described in Patients from the Republic of Macedonia. Hemoglobin 41:4-6, pages 308-310.
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Felix de la Fuente-Gonzalo, Montserrat Baiget, Isabel Badell, Pilar Ricard, Lara Vinuesa, Jorge Martínez-Nieto, Paloma Ropero, Ana Villegas, Fernando A. González, Joaquin Díaz-Mediavilla & The Erythropathology Spanish Group. (2012) Study of Three Families with Hb Agrinio [α29(B10)Leu→Pro, CTG>CCG (α2)] in the Spanish Population: Three Homozygous Cases. Hemoglobin 36:6, pages 526-532.
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Aspasia Destouni, George Christopoulos, Christina Vrettou, Georgia Kakourou, Marina Kleanthous, Jan Traeger-Synodinos & Emmanuel Kanavakis. (2012) Microsatellite Markers Within the α-Globin Gene Cluster for Robust Preimplantation Genetic Diagnosis of Severe α-Thalassemia Syndromes in Mediterranean Populations. Hemoglobin 36:3, pages 253-264.
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Joanne Traeger-Synodinos, Varvara Douna, Ioannis Papassotiriou, Alexandra Stamoulakatou, Vasilis Ladis, Tania Siahanidou, Irine Fylaktou & Emmanuel Kanavakis. (2010) Variable and Often Severe Phenotypic Expression in Patients with the α-Thalassemic Variant Hb Agrinio [α29(B10)Leu→Pro (α2)]. Hemoglobin 34:5, pages 430-438.
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Varvara Douna, Ioannis Papassotiriou, Alexandra Stamoulakatou, Anna Metaxotou-Mavrommati, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2008) Association of Mild and Severely Unstable α Chain Variants: The First Observation of a Compound Heterozygote with Hb Setif [α94(G1)Asp→Tyr (α2)] and Hb Agrinio [α29(B10)Leu→Pro (α2)] in a Greek Family. Hemoglobin 32:6, pages 592-595.
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Articles from other publishers (8)

Michael D. Diamantidis, Stefania Pitsava, Omar Zayed, Ioanna Argyrakouli, Konstantinos Karapiperis, Christos Chatzoulis, Evangelos Alexiou, Achilles Manafas, Evangelos Tsangalas & Konstantinos Karakoussis. (2023) Concomitant Presence of Hb Agrinio and - -Med Deletion in a Greek Male Patient with Hemoglobinopathy H: More Severe Phenotype and Literature Review. Hematology Reports 15:3, pages 483-490.
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Sarah Szepetowski, Claire Berger, Philippe Joly, Sandrine Baron‐Joly, Yoann Huguenin, Aurélie Cantais, Sophie Brun, Cécile Ged, Catherine Badens, Isabelle Thuret, Muriel Giansily‐Blaizot, Serge Pissard & Patricia Aguilar‐Martinez. (2022) Homozygosity for the hyperunstable hemoglobin variant Hb Agrinio ( HBA2 :c. 89T >C) leads to severe antenatal anemia: Eight new cases in three families . American Journal of Hematology 97:11.
Crossref
Herminio López-Escribano & Ausias Hervás-Romero. (2021) Study of alpha-thalassemia in the clinical laboratory: genotypes-phenotypes of clinical interest and their diagnostic approach. Revista de Medicina de Laboratorio.
Crossref
Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 85 184 .
David Gazzaniga, Ashley Brenton & Brian Meshkin. (2017) A precision medicine approach to a patient with unresolved pain following orthopedic surgery: a case report. Journal of Medical Case Reports 11:1.
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Petros Kountouris, Ioanna Kousiappa, Thessalia Papasavva, George Christopoulos, Eleni Pavlou, Miranda Petrou, Xenia Feleki, Eleni Karitzie, Marios Phylactides, Pavlos Fanis, Carsten W. Lederer, Andreani R. Kyrri, Eleni Kalogerou, Christiana Makariou, Christiana Ioannou, Loukas Kythreotis, Georgia Hadjilambi, Nicoletta Andreou, Evangelia Pangalou, Irene Savvidou, Michael Angastiniotis, Michael Hadjigavriel, Maria Sitarou, Annita Kolnagou, Marina Kleanthous & Soteroula Christou. (2016) The molecular spectrum and distribution of haemoglobinopathies in Cyprus: a 20-year retrospective study. Scientific Reports 6:1.
Crossref
Berndt Zur. (2016) Hemoglobin variants – pathomechanism, symptoms and diagnosis. LaboratoriumsMedizin 39:s1.
Crossref
Berndt Zur. (2015) Hämoglobinvarianten – Pathomechanismus, Symptome und Diagnostik. LaboratoriumsMedizin 39:5, pages 311-324.
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