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The first case of 38,XX (SRY-positive) disorder of sex development in a cat
BACKGROUND: SRY-positive XX testicular disorder of sex development (DSD) caused by X;Y translocations was not yet reported in domestic animals. In humans it is rarely diagnosed and a majority of clinical features resemble those which are typical for Klinefelter syndrome (KS). Here we describe the fi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382857/ https://www.ncbi.nlm.nih.gov/pubmed/25838845 http://dx.doi.org/10.1186/s13039-015-0128-5 |
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author | Szczerbal, Izabela Stachowiak, Monika Dzimira, Stanislaw Sliwa, Krystyna Switonski, Marek |
author_facet | Szczerbal, Izabela Stachowiak, Monika Dzimira, Stanislaw Sliwa, Krystyna Switonski, Marek |
author_sort | Szczerbal, Izabela |
collection | PubMed |
description | BACKGROUND: SRY-positive XX testicular disorder of sex development (DSD) caused by X;Y translocations was not yet reported in domestic animals. In humans it is rarely diagnosed and a majority of clinical features resemble those which are typical for Klinefelter syndrome (KS). Here we describe the first case of SRY-positive XX DSD in a tortoiseshell cat with a rudimentary penis and a lack of scrotum. RESULTS: Molecular analysis showed the presence of two Y-linked genes (SRY and ZFY) and a normal sequence of the SRY gene. Application of classical cytogenetic techniques revealed two X chromosomes (38,XX), but further FISH studies with the use of the whole X chromosome painting probe and BAC probes specific to the Yp chromosome facilitated identification of Xp;Yp translocation. The SRY gene was localised at a distal position of Xp. The karyotype of the studied case was described as: 38,XX.ish der(X)t(X;Y)(p22;p12)(SRY+). Moreover, the X inactivation status assessed by a sequential R-banding and FISH with the SRY-specific probe showed a random inactivation of the derivative X(SRY) chromosome. CONCLUSIONS: Our study showed that among DSD tortoiseshell cats, apart from XXY trisomy and XX/XY chimerism, also SRY-positive XX cases may occur. It is hypothesized that the extremely rare occurrence of this abnormality in domestic animals, when compared with humans, may be associated with a different organisation of the Yp arm in these species. |
format | Online Article Text |
id | pubmed-4382857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43828572015-04-03 The first case of 38,XX (SRY-positive) disorder of sex development in a cat Szczerbal, Izabela Stachowiak, Monika Dzimira, Stanislaw Sliwa, Krystyna Switonski, Marek Mol Cytogenet Case Report BACKGROUND: SRY-positive XX testicular disorder of sex development (DSD) caused by X;Y translocations was not yet reported in domestic animals. In humans it is rarely diagnosed and a majority of clinical features resemble those which are typical for Klinefelter syndrome (KS). Here we describe the first case of SRY-positive XX DSD in a tortoiseshell cat with a rudimentary penis and a lack of scrotum. RESULTS: Molecular analysis showed the presence of two Y-linked genes (SRY and ZFY) and a normal sequence of the SRY gene. Application of classical cytogenetic techniques revealed two X chromosomes (38,XX), but further FISH studies with the use of the whole X chromosome painting probe and BAC probes specific to the Yp chromosome facilitated identification of Xp;Yp translocation. The SRY gene was localised at a distal position of Xp. The karyotype of the studied case was described as: 38,XX.ish der(X)t(X;Y)(p22;p12)(SRY+). Moreover, the X inactivation status assessed by a sequential R-banding and FISH with the SRY-specific probe showed a random inactivation of the derivative X(SRY) chromosome. CONCLUSIONS: Our study showed that among DSD tortoiseshell cats, apart from XXY trisomy and XX/XY chimerism, also SRY-positive XX cases may occur. It is hypothesized that the extremely rare occurrence of this abnormality in domestic animals, when compared with humans, may be associated with a different organisation of the Yp arm in these species. BioMed Central 2015-03-26 /pmc/articles/PMC4382857/ /pubmed/25838845 http://dx.doi.org/10.1186/s13039-015-0128-5 Text en © Szczerbal et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Szczerbal, Izabela Stachowiak, Monika Dzimira, Stanislaw Sliwa, Krystyna Switonski, Marek The first case of 38,XX (SRY-positive) disorder of sex development in a cat |
title | The first case of 38,XX (SRY-positive) disorder of sex development in a cat |
title_full | The first case of 38,XX (SRY-positive) disorder of sex development in a cat |
title_fullStr | The first case of 38,XX (SRY-positive) disorder of sex development in a cat |
title_full_unstemmed | The first case of 38,XX (SRY-positive) disorder of sex development in a cat |
title_short | The first case of 38,XX (SRY-positive) disorder of sex development in a cat |
title_sort | first case of 38,xx (sry-positive) disorder of sex development in a cat |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382857/ https://www.ncbi.nlm.nih.gov/pubmed/25838845 http://dx.doi.org/10.1186/s13039-015-0128-5 |
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