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Rare 48, XYYY syndrome: case report and review of the literature
48, XYYY syndrome is a rare condition. A male with 32‐year‐old and three Y chromosomes is described. This syndrome is phenotypically similar to Klinefelter syndrome. In this patient, Semi‐Klinefelter characteristics such as tall stature, teeth dysmorphology, long length of fingers, partial deformity...
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/PMC5771943/ https://www.ncbi.nlm.nih.gov/pubmed/29375860 http://dx.doi.org/10.1002/ccr3.1311 |
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author | Abedi, Maryam Salmaninejad, Arash Sakhinia, Ebrahim |
author_facet | Abedi, Maryam Salmaninejad, Arash Sakhinia, Ebrahim |
author_sort | Abedi, Maryam |
collection | PubMed |
description | 48, XYYY syndrome is a rare condition. A male with 32‐year‐old and three Y chromosomes is described. This syndrome is phenotypically similar to Klinefelter syndrome. In this patient, Semi‐Klinefelter characteristics such as tall stature, teeth dysmorphology, long length of fingers, partial deformity of the joints, likewise mental health problems were obvious. |
format | Online Article Text |
id | pubmed-5771943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57719432018-01-26 Rare 48, XYYY syndrome: case report and review of the literature Abedi, Maryam Salmaninejad, Arash Sakhinia, Ebrahim Clin Case Rep Case Reports 48, XYYY syndrome is a rare condition. A male with 32‐year‐old and three Y chromosomes is described. This syndrome is phenotypically similar to Klinefelter syndrome. In this patient, Semi‐Klinefelter characteristics such as tall stature, teeth dysmorphology, long length of fingers, partial deformity of the joints, likewise mental health problems were obvious. John Wiley and Sons Inc. 2017-12-07 /pmc/articles/PMC5771943/ /pubmed/29375860 http://dx.doi.org/10.1002/ccr3.1311 Text en © 2017 The Authors. 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 Abedi, Maryam Salmaninejad, Arash Sakhinia, Ebrahim Rare 48, XYYY syndrome: case report and review of the literature |
title | Rare 48, XYYY syndrome: case report and review of the literature |
title_full | Rare 48, XYYY syndrome: case report and review of the literature |
title_fullStr | Rare 48, XYYY syndrome: case report and review of the literature |
title_full_unstemmed | Rare 48, XYYY syndrome: case report and review of the literature |
title_short | Rare 48, XYYY syndrome: case report and review of the literature |
title_sort | rare 48, xyyy syndrome: case report and review of the literature |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771943/ https://www.ncbi.nlm.nih.gov/pubmed/29375860 http://dx.doi.org/10.1002/ccr3.1311 |
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