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Tetraploid–diploid mosaicism in a patient with pigmentary anomalies of hair and skin: a new dermatologic feature
Tetraploid–diploid mosaicism in humans is exceedingly rare. We present an 11‐year‐old boy with tetraploid–diploid mosaicism and coexistent hair hypopigmentation with skin hypo‐ and hyperpigmentation. This case expands the current literature as we are not aware of previous documentation of this uniqu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771914/ https://www.ncbi.nlm.nih.gov/pubmed/29375847 http://dx.doi.org/10.1002/ccr3.1114 |
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author | Schacht, John Paul Farnworth, Elisha Hogue, Jacob Rohena, Luis |
author_facet | Schacht, John Paul Farnworth, Elisha Hogue, Jacob Rohena, Luis |
author_sort | Schacht, John Paul |
collection | PubMed |
description | Tetraploid–diploid mosaicism in humans is exceedingly rare. We present an 11‐year‐old boy with tetraploid–diploid mosaicism and coexistent hair hypopigmentation with skin hypo‐ and hyperpigmentation. This case expands the current literature as we are not aware of previous documentation of this unique combination of pigmentary anomalies. |
format | Online Article Text |
id | pubmed-5771914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57719142018-01-26 Tetraploid–diploid mosaicism in a patient with pigmentary anomalies of hair and skin: a new dermatologic feature Schacht, John Paul Farnworth, Elisha Hogue, Jacob Rohena, Luis Clin Case Rep Case Reports Tetraploid–diploid mosaicism in humans is exceedingly rare. We present an 11‐year‐old boy with tetraploid–diploid mosaicism and coexistent hair hypopigmentation with skin hypo‐ and hyperpigmentation. This case expands the current literature as we are not aware of previous documentation of this unique combination of pigmentary anomalies. John Wiley and Sons Inc. 2017-11-29 /pmc/articles/PMC5771914/ /pubmed/29375847 http://dx.doi.org/10.1002/ccr3.1114 Text en Published 2017. This article is a U.S. Government work and is in the public domain in the USA. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Schacht, John Paul Farnworth, Elisha Hogue, Jacob Rohena, Luis Tetraploid–diploid mosaicism in a patient with pigmentary anomalies of hair and skin: a new dermatologic feature |
title | Tetraploid–diploid mosaicism in a patient with pigmentary anomalies of hair and skin: a new dermatologic feature |
title_full | Tetraploid–diploid mosaicism in a patient with pigmentary anomalies of hair and skin: a new dermatologic feature |
title_fullStr | Tetraploid–diploid mosaicism in a patient with pigmentary anomalies of hair and skin: a new dermatologic feature |
title_full_unstemmed | Tetraploid–diploid mosaicism in a patient with pigmentary anomalies of hair and skin: a new dermatologic feature |
title_short | Tetraploid–diploid mosaicism in a patient with pigmentary anomalies of hair and skin: a new dermatologic feature |
title_sort | tetraploid–diploid mosaicism in a patient with pigmentary anomalies of hair and skin: a new dermatologic feature |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771914/ https://www.ncbi.nlm.nih.gov/pubmed/29375847 http://dx.doi.org/10.1002/ccr3.1114 |
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