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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...

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Autores principales: Szczerbal, Izabela, Stachowiak, Monika, Dzimira, Stanislaw, Sliwa, Krystyna, Switonski, Marek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
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.
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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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