首页> 外文期刊>Sexual development: genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation >Disorders of Sex Development Are an Emerging Problem in French Bulldogs: A Description of Six New Cases and a Review of the Literature
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Disorders of Sex Development Are an Emerging Problem in French Bulldogs: A Description of Six New Cases and a Review of the Literature

机译:性发展障碍是法国斗牛犬的新出现问题:对六个新病例的描述以及对文献的审查

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Disorders of sex development (DSD) are a well-known cause of sterility and reduced fertility in dogs. Here, we report on 6 new cases of DSD in French bulldogs diagnosed by us within the last year. The animals were phenotypical females who underwent detailed diagnosis due to the presence of an enlarged clitoris or a penis-like structure with atypically located urethral orifice (hypospadias). A female karyotype (78,XX) and lack of Y-linked genes (SRY and ZFY) were observed in 5 cases, which were classified as XX (SRY-negative) DSD. Go-nads histology could be performed in 4 XX DSD cases: tes-ticular tissue was observed in 3 cases and ovotesticular tissue in 1 case. In the last case, leukocyte chimerism (XX/XY) was detected alongside an ovotestis with epididymis and fallopian tubes. This case was classified as freemartinism. Our study and a literature review showed that heritable XX (SRY-negative) DSD is quite common in French bulldogs, but spontaneously developed freemartinism can be also diagnosed. In conclusion, we postulate that the description of the sexual phenotype of DSD females (enlarged clitoris and presence of testicular tissue) does not distinguish between hereditary XX DSD and nonhereditary freemartinism. Cyto-genetic and molecular analyses are thus necessary to correctly diagnose such cases. This is especially important for the French bulldog breed, as a rapid increase in its population could spread hereditary DSD.
机译:性发展障碍(DSD)是众所周知的无菌原因,并在狗的生育率降低。在这里,我们在去年在美国诊断的法国斗牛犬中报告了6例DSD新案例。由于存在扩大的阴蒂或阴茎状结构,这些动物是表型女性,其接受了详细的诊断,这些诊断具有扩大的阴蒂或阴茎状结构,其具有非型尿道孔口(Hypospadias)。在5例中观察到雌性核型(78,XX)和缺乏Y型链接基因(SRY和ZFY),其被分类为XX(Sry-Digal)DSD。 Go-NADS组织学可以在4例XX DSD案例中进行:在3例和卵巢组织中观察到TES-TICURAL COADION 1例。在最后一个情况下,与附睾和输卵管的卵巢伴有卵巢检测白细胞嵌合(XX / XY)。本案例被归类为弗里西哲学。我们的研究和文献综述表明,遗传的XX(Sry-Digal)DSD在法国斗牛犬中非常常见,但也可以诊断出来的自发性发达的弗里西术主义。总之,我们假设DSD女性的性表型(阴蒂和睾丸组织的存在)的描述并不区分遗传XX DSD和非秘密的弗里德术。因此需要细胞遗传和分子分析来正确诊断这种情况。这对法国斗牛犬品种尤为重要,因为其人口的迅速增加可能会传播遗传性DSD。

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