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Diamond Blackfan Anemia: a Tertiary Care Center Experience
Diamond Blackfan Anemia (DBA) is a rare hypoplastic anemia that presents in infancy with macrocytic anemia and reticulocytopenia. It is a ribosomopathy with autosomal dominant inheritance. In our series of 10 patients with DBA, congenital malformations were observed in 50% of the cases. Age at sympt...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Università Cattolica del Sacro Cuore
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684352/ https://www.ncbi.nlm.nih.gov/pubmed/23795277 http://dx.doi.org/10.4084/MJHID.2013.039 |
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author | Singh, Avinash Kumar Radhakrishnan, Nita Seth, Tulika Mishra, Pravas Mahapatra, Manoranjan Pati, Haraprasad |
author_facet | Singh, Avinash Kumar Radhakrishnan, Nita Seth, Tulika Mishra, Pravas Mahapatra, Manoranjan Pati, Haraprasad |
author_sort | Singh, Avinash Kumar |
collection | PubMed |
description | Diamond Blackfan Anemia (DBA) is a rare hypoplastic anemia that presents in infancy with macrocytic anemia and reticulocytopenia. It is a ribosomopathy with autosomal dominant inheritance. In our series of 10 patients with DBA, congenital malformations were observed in 50% of the cases. Age at symptom onset ranged from 0–12 months. Age at diagnosis ranged from 4 months to 96 months. Male: female ratio was 9:1. Response to prednisolone was observed in 4 out of the 10 patients (either during initial treatment or during re-challenge). Response to cyclosporine was found to be poor. Bone marrow transplantation was successful in attaining remission in one patient. Malignancies were not reported in any patient possibly due to a short follow up period. |
format | Online Article Text |
id | pubmed-3684352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Università Cattolica del Sacro Cuore |
record_format | MEDLINE/PubMed |
spelling | pubmed-36843522013-06-21 Diamond Blackfan Anemia: a Tertiary Care Center Experience Singh, Avinash Kumar Radhakrishnan, Nita Seth, Tulika Mishra, Pravas Mahapatra, Manoranjan Pati, Haraprasad Mediterr J Hematol Infect Dis Original Article Diamond Blackfan Anemia (DBA) is a rare hypoplastic anemia that presents in infancy with macrocytic anemia and reticulocytopenia. It is a ribosomopathy with autosomal dominant inheritance. In our series of 10 patients with DBA, congenital malformations were observed in 50% of the cases. Age at symptom onset ranged from 0–12 months. Age at diagnosis ranged from 4 months to 96 months. Male: female ratio was 9:1. Response to prednisolone was observed in 4 out of the 10 patients (either during initial treatment or during re-challenge). Response to cyclosporine was found to be poor. Bone marrow transplantation was successful in attaining remission in one patient. Malignancies were not reported in any patient possibly due to a short follow up period. Università Cattolica del Sacro Cuore 2013-06-03 /pmc/articles/PMC3684352/ /pubmed/23795277 http://dx.doi.org/10.4084/MJHID.2013.039 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Singh, Avinash Kumar Radhakrishnan, Nita Seth, Tulika Mishra, Pravas Mahapatra, Manoranjan Pati, Haraprasad Diamond Blackfan Anemia: a Tertiary Care Center Experience |
title | Diamond Blackfan Anemia: a Tertiary Care Center Experience |
title_full | Diamond Blackfan Anemia: a Tertiary Care Center Experience |
title_fullStr | Diamond Blackfan Anemia: a Tertiary Care Center Experience |
title_full_unstemmed | Diamond Blackfan Anemia: a Tertiary Care Center Experience |
title_short | Diamond Blackfan Anemia: a Tertiary Care Center Experience |
title_sort | diamond blackfan anemia: a tertiary care center experience |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684352/ https://www.ncbi.nlm.nih.gov/pubmed/23795277 http://dx.doi.org/10.4084/MJHID.2013.039 |
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