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The phenotype of a pig with monosomy X resembling Turner syndrome symptoms: a case report
The partial or complete loss of one X chromosome in humans causes Turner syndrome (TS), which is accompanied by a range of physical and reproductive pathologies. This article reports similarities between the phenotype of a pig with monosomy X and the symptoms of TS in humans. Born as the offspring o...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Society for Reproduction and Development
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584175/ https://www.ncbi.nlm.nih.gov/pubmed/30773506 http://dx.doi.org/10.1262/jrd.2018-143 |
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author | UMEYAMA, Kazuhiro NAKANO, Kazuaki MATSUNARI, Hitomi YAMADA, Takeshi HASEGAWA, Koki TANG, Kun TOKUYAMA, Yuki WATANABE, Masahito NAGAYA, Masaki NAGASHIMA, Hiroshi |
author_facet | UMEYAMA, Kazuhiro NAKANO, Kazuaki MATSUNARI, Hitomi YAMADA, Takeshi HASEGAWA, Koki TANG, Kun TOKUYAMA, Yuki WATANABE, Masahito NAGAYA, Masaki NAGASHIMA, Hiroshi |
author_sort | UMEYAMA, Kazuhiro |
collection | PubMed |
description | The partial or complete loss of one X chromosome in humans causes Turner syndrome (TS), which is accompanied by a range of physical and reproductive pathologies. This article reports similarities between the phenotype of a pig with monosomy X and the symptoms of TS in humans. Born as the offspring of a male pig carrying a mutation in an X-chromosomal gene, ornithine transcarbamylase (OTC), the female pig (37,XO) was raised to the age of 36 months. This X-monosomic pig presented with abnormal physical characteristics including short stature, micrognathia, and skeletal abnormalities in the limbs. Furthermore, the female did not exhibit an estrous cycle, even after reaching the age of sexual maturity, and showed no ovarian endocrine activity except for an irregular increase in blood 17β-estradiol levels, which was seemingly attributable to sporadic follicular development. An autopsy at 36 months revealed an undeveloped reproductive tract with ovaries that lacked follicles. These data demonstrated that the growth processes and anatomical and physiological characteristics of an X-monosomic pig closely resembled those of a human with TS. |
format | Online Article Text |
id | pubmed-6584175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Society for Reproduction and Development |
record_format | MEDLINE/PubMed |
spelling | pubmed-65841752019-06-25 The phenotype of a pig with monosomy X resembling Turner syndrome symptoms: a case report UMEYAMA, Kazuhiro NAKANO, Kazuaki MATSUNARI, Hitomi YAMADA, Takeshi HASEGAWA, Koki TANG, Kun TOKUYAMA, Yuki WATANABE, Masahito NAGAYA, Masaki NAGASHIMA, Hiroshi J Reprod Dev Original Article The partial or complete loss of one X chromosome in humans causes Turner syndrome (TS), which is accompanied by a range of physical and reproductive pathologies. This article reports similarities between the phenotype of a pig with monosomy X and the symptoms of TS in humans. Born as the offspring of a male pig carrying a mutation in an X-chromosomal gene, ornithine transcarbamylase (OTC), the female pig (37,XO) was raised to the age of 36 months. This X-monosomic pig presented with abnormal physical characteristics including short stature, micrognathia, and skeletal abnormalities in the limbs. Furthermore, the female did not exhibit an estrous cycle, even after reaching the age of sexual maturity, and showed no ovarian endocrine activity except for an irregular increase in blood 17β-estradiol levels, which was seemingly attributable to sporadic follicular development. An autopsy at 36 months revealed an undeveloped reproductive tract with ovaries that lacked follicles. These data demonstrated that the growth processes and anatomical and physiological characteristics of an X-monosomic pig closely resembled those of a human with TS. The Society for Reproduction and Development 2019-02-15 2019-06 /pmc/articles/PMC6584175/ /pubmed/30773506 http://dx.doi.org/10.1262/jrd.2018-143 Text en ©2019 Society for Reproduction and Development This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Original Article UMEYAMA, Kazuhiro NAKANO, Kazuaki MATSUNARI, Hitomi YAMADA, Takeshi HASEGAWA, Koki TANG, Kun TOKUYAMA, Yuki WATANABE, Masahito NAGAYA, Masaki NAGASHIMA, Hiroshi The phenotype of a pig with monosomy X resembling Turner syndrome symptoms: a case report |
title | The phenotype of a pig with monosomy X resembling Turner syndrome symptoms: a case report |
title_full | The phenotype of a pig with monosomy X resembling Turner syndrome symptoms: a case report |
title_fullStr | The phenotype of a pig with monosomy X resembling Turner syndrome symptoms: a case report |
title_full_unstemmed | The phenotype of a pig with monosomy X resembling Turner syndrome symptoms: a case report |
title_short | The phenotype of a pig with monosomy X resembling Turner syndrome symptoms: a case report |
title_sort | phenotype of a pig with monosomy x resembling turner syndrome symptoms: a case report |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584175/ https://www.ncbi.nlm.nih.gov/pubmed/30773506 http://dx.doi.org/10.1262/jrd.2018-143 |
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