Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Abedi, Maryam, Salmaninejad, Arash, Sakhinia, Ebrahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
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
_version_ 1783293328383541248
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
work_keys_str_mv AT abedimaryam rare48xyyysyndromecasereportandreviewoftheliterature
AT salmaninejadarash rare48xyyysyndromecasereportandreviewoftheliterature
AT sakhiniaebrahim rare48xyyysyndromecasereportandreviewoftheliterature