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Transient Abnormal Myelopoeisis and Mosaic down Syndrome in a Phenotypically Normal Newborn

Transient abnormal myelopoiesis (TAM) is a common and potentially fatal neonatal complication of newborn babies with Down syndrome (DS). Children born with mosaic DS are also at risk of developing TAM. However, due to their variable phenotypes, early identification of patients with mosaic DS may be...

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Autores principales: Prudowsky, Zachary, Han, HyoJeong, Stevens, Alexandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346181/
https://www.ncbi.nlm.nih.gov/pubmed/32481622
http://dx.doi.org/10.3390/children7060052
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author Prudowsky, Zachary
Han, HyoJeong
Stevens, Alexandra
author_facet Prudowsky, Zachary
Han, HyoJeong
Stevens, Alexandra
author_sort Prudowsky, Zachary
collection PubMed
description Transient abnormal myelopoiesis (TAM) is a common and potentially fatal neonatal complication of newborn babies with Down syndrome (DS). Children born with mosaic DS are also at risk of developing TAM. However, due to their variable phenotypes, early identification of patients with mosaic DS may be difficult; thus, early diagnosis of TAM is just as challenging. In this report, we describe a case of a phenotypically normal newborn who presented with concerns for neonatal leukemia. The diagnosis of mosaic DS and TAM was confirmed with abnormal GATA1 mutation testing, highlighting the importance of early GATA1 mutation testing in newborn leukemia with high suspicion for TAM.
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spelling pubmed-73461812020-07-14 Transient Abnormal Myelopoeisis and Mosaic down Syndrome in a Phenotypically Normal Newborn Prudowsky, Zachary Han, HyoJeong Stevens, Alexandra Children (Basel) Case Report Transient abnormal myelopoiesis (TAM) is a common and potentially fatal neonatal complication of newborn babies with Down syndrome (DS). Children born with mosaic DS are also at risk of developing TAM. However, due to their variable phenotypes, early identification of patients with mosaic DS may be difficult; thus, early diagnosis of TAM is just as challenging. In this report, we describe a case of a phenotypically normal newborn who presented with concerns for neonatal leukemia. The diagnosis of mosaic DS and TAM was confirmed with abnormal GATA1 mutation testing, highlighting the importance of early GATA1 mutation testing in newborn leukemia with high suspicion for TAM. MDPI 2020-05-28 /pmc/articles/PMC7346181/ /pubmed/32481622 http://dx.doi.org/10.3390/children7060052 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Prudowsky, Zachary
Han, HyoJeong
Stevens, Alexandra
Transient Abnormal Myelopoeisis and Mosaic down Syndrome in a Phenotypically Normal Newborn
title Transient Abnormal Myelopoeisis and Mosaic down Syndrome in a Phenotypically Normal Newborn
title_full Transient Abnormal Myelopoeisis and Mosaic down Syndrome in a Phenotypically Normal Newborn
title_fullStr Transient Abnormal Myelopoeisis and Mosaic down Syndrome in a Phenotypically Normal Newborn
title_full_unstemmed Transient Abnormal Myelopoeisis and Mosaic down Syndrome in a Phenotypically Normal Newborn
title_short Transient Abnormal Myelopoeisis and Mosaic down Syndrome in a Phenotypically Normal Newborn
title_sort transient abnormal myelopoeisis and mosaic down syndrome in a phenotypically normal newborn
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346181/
https://www.ncbi.nlm.nih.gov/pubmed/32481622
http://dx.doi.org/10.3390/children7060052
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AT stevensalexandra transientabnormalmyelopoeisisandmosaicdownsyndromeinaphenotypicallynormalnewborn