A case of congenital dyserythropoietic anemia type IV

Congenital dyserythropoietic anemias (CDAs) are displayed by ineffective erythropoiesis. The wide variety of phenotypes observed in CDA patients makes differential diagnosis difficult; identification of the genetic variants is crucial in clinical management. We report the fifth case of a patient wit...

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Autores principales: de‐ la‐ Iglesia‐ Iñigo, Silvia, Moreno‐Carralero, María‐Isabel, Lemes‐Castellano, Angelina, Molero‐Labarta, Teresa, Méndez, Manuel, Morán‐Jiménez, María‐José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331261/
https://www.ncbi.nlm.nih.gov/pubmed/28265383
http://dx.doi.org/10.1002/ccr3.825
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author de‐ la‐ Iglesia‐ Iñigo, Silvia
Moreno‐Carralero, María‐Isabel
Lemes‐Castellano, Angelina
Molero‐Labarta, Teresa
Méndez, Manuel
Morán‐Jiménez, María‐José
author_facet de‐ la‐ Iglesia‐ Iñigo, Silvia
Moreno‐Carralero, María‐Isabel
Lemes‐Castellano, Angelina
Molero‐Labarta, Teresa
Méndez, Manuel
Morán‐Jiménez, María‐José
author_sort de‐ la‐ Iglesia‐ Iñigo, Silvia
collection PubMed
description Congenital dyserythropoietic anemias (CDAs) are displayed by ineffective erythropoiesis. The wide variety of phenotypes observed in CDA patients makes differential diagnosis difficult; identification of the genetic variants is crucial in clinical management. We report the fifth case of a patient with unclassified CDAs, after genetic study, with CDA type IV.
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spelling pubmed-53312612017-03-06 A case of congenital dyserythropoietic anemia type IV de‐ la‐ Iglesia‐ Iñigo, Silvia Moreno‐Carralero, María‐Isabel Lemes‐Castellano, Angelina Molero‐Labarta, Teresa Méndez, Manuel Morán‐Jiménez, María‐José Clin Case Rep Case Reports Congenital dyserythropoietic anemias (CDAs) are displayed by ineffective erythropoiesis. The wide variety of phenotypes observed in CDA patients makes differential diagnosis difficult; identification of the genetic variants is crucial in clinical management. We report the fifth case of a patient with unclassified CDAs, after genetic study, with CDA type IV. John Wiley and Sons Inc. 2017-01-28 /pmc/articles/PMC5331261/ /pubmed/28265383 http://dx.doi.org/10.1002/ccr3.825 Text en © 2017 The Authors Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Reports
de‐ la‐ Iglesia‐ Iñigo, Silvia
Moreno‐Carralero, María‐Isabel
Lemes‐Castellano, Angelina
Molero‐Labarta, Teresa
Méndez, Manuel
Morán‐Jiménez, María‐José
A case of congenital dyserythropoietic anemia type IV
title A case of congenital dyserythropoietic anemia type IV
title_full A case of congenital dyserythropoietic anemia type IV
title_fullStr A case of congenital dyserythropoietic anemia type IV
title_full_unstemmed A case of congenital dyserythropoietic anemia type IV
title_short A case of congenital dyserythropoietic anemia type IV
title_sort case of congenital dyserythropoietic anemia type iv
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331261/
https://www.ncbi.nlm.nih.gov/pubmed/28265383
http://dx.doi.org/10.1002/ccr3.825
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