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Transient abnormal myelopoiesis in pediatrics with trisomy 21
Transient abnormal myelopoiesis is common among Down syndrome patients. Although no therapeutic measures are required, close monitoring of comorbidities such as gastrointestinal bleeding is required. Long‐term follow‐up is promising for a healthy future and reduced requirement of unnecessary therape...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869390/ https://www.ncbi.nlm.nih.gov/pubmed/33598211 http://dx.doi.org/10.1002/ccr3.3589 |
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author | Taee, Nadereh Faraji‐Goodarzi, Mojgan Safdari, Mohammad Bajelan, Amir |
author_facet | Taee, Nadereh Faraji‐Goodarzi, Mojgan Safdari, Mohammad Bajelan, Amir |
author_sort | Taee, Nadereh |
collection | PubMed |
description | Transient abnormal myelopoiesis is common among Down syndrome patients. Although no therapeutic measures are required, close monitoring of comorbidities such as gastrointestinal bleeding is required. Long‐term follow‐up is promising for a healthy future and reduced requirement of unnecessary therapeutic measures including chemotherapy and remission of the pathology. |
format | Online Article Text |
id | pubmed-7869390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78693902021-02-16 Transient abnormal myelopoiesis in pediatrics with trisomy 21 Taee, Nadereh Faraji‐Goodarzi, Mojgan Safdari, Mohammad Bajelan, Amir Clin Case Rep Case Reports Transient abnormal myelopoiesis is common among Down syndrome patients. Although no therapeutic measures are required, close monitoring of comorbidities such as gastrointestinal bleeding is required. Long‐term follow‐up is promising for a healthy future and reduced requirement of unnecessary therapeutic measures including chemotherapy and remission of the pathology. John Wiley and Sons Inc. 2020-11-29 /pmc/articles/PMC7869390/ /pubmed/33598211 http://dx.doi.org/10.1002/ccr3.3589 Text en © 2020 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the 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 Taee, Nadereh Faraji‐Goodarzi, Mojgan Safdari, Mohammad Bajelan, Amir Transient abnormal myelopoiesis in pediatrics with trisomy 21 |
title | Transient abnormal myelopoiesis in pediatrics with trisomy 21 |
title_full | Transient abnormal myelopoiesis in pediatrics with trisomy 21 |
title_fullStr | Transient abnormal myelopoiesis in pediatrics with trisomy 21 |
title_full_unstemmed | Transient abnormal myelopoiesis in pediatrics with trisomy 21 |
title_short | Transient abnormal myelopoiesis in pediatrics with trisomy 21 |
title_sort | transient abnormal myelopoiesis in pediatrics with trisomy 21 |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869390/ https://www.ncbi.nlm.nih.gov/pubmed/33598211 http://dx.doi.org/10.1002/ccr3.3589 |
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