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Allogeneic HSCT in Adolescents and Young Adults With Primary Immunodeficiencies
Significant advances in hematopoietic transplantation over the past 20 years, have facilitated the safe transplantation of older adults with higher co-morbidities. In pediatric practice these advances have simultaneously improved outcomes for sicker children with complex, rare diseases including the...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821713/ https://www.ncbi.nlm.nih.gov/pubmed/31709207 http://dx.doi.org/10.3389/fped.2019.00437 |
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author | Morris, Emma C. Albert, Michael H. |
author_facet | Morris, Emma C. Albert, Michael H. |
author_sort | Morris, Emma C. |
collection | PubMed |
description | Significant advances in hematopoietic transplantation over the past 20 years, have facilitated the safe transplantation of older adults with higher co-morbidities. In pediatric practice these advances have simultaneously improved outcomes for sicker children with complex, rare diseases including the primary immunodeficiencies, PID. With more widespread adoption of genetic sequencing, older patients with disease-causing mutations restricted to the hematopoietic system can be identified who may benefit from allogeneic hematopoietic stem cell transplantation (Allo-HSCT). Here we discuss the evidence for Allo-HSCT in adolescent and younger adults (AYAs) with PID. |
format | Online Article Text |
id | pubmed-6821713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68217132019-11-08 Allogeneic HSCT in Adolescents and Young Adults With Primary Immunodeficiencies Morris, Emma C. Albert, Michael H. Front Pediatr Pediatrics Significant advances in hematopoietic transplantation over the past 20 years, have facilitated the safe transplantation of older adults with higher co-morbidities. In pediatric practice these advances have simultaneously improved outcomes for sicker children with complex, rare diseases including the primary immunodeficiencies, PID. With more widespread adoption of genetic sequencing, older patients with disease-causing mutations restricted to the hematopoietic system can be identified who may benefit from allogeneic hematopoietic stem cell transplantation (Allo-HSCT). Here we discuss the evidence for Allo-HSCT in adolescent and younger adults (AYAs) with PID. Frontiers Media S.A. 2019-10-24 /pmc/articles/PMC6821713/ /pubmed/31709207 http://dx.doi.org/10.3389/fped.2019.00437 Text en Copyright © 2019 Morris and Albert. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pediatrics Morris, Emma C. Albert, Michael H. Allogeneic HSCT in Adolescents and Young Adults With Primary Immunodeficiencies |
title | Allogeneic HSCT in Adolescents and Young Adults With Primary Immunodeficiencies |
title_full | Allogeneic HSCT in Adolescents and Young Adults With Primary Immunodeficiencies |
title_fullStr | Allogeneic HSCT in Adolescents and Young Adults With Primary Immunodeficiencies |
title_full_unstemmed | Allogeneic HSCT in Adolescents and Young Adults With Primary Immunodeficiencies |
title_short | Allogeneic HSCT in Adolescents and Young Adults With Primary Immunodeficiencies |
title_sort | allogeneic hsct in adolescents and young adults with primary immunodeficiencies |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821713/ https://www.ncbi.nlm.nih.gov/pubmed/31709207 http://dx.doi.org/10.3389/fped.2019.00437 |
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