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首页> 外文期刊>BMC Veterinary Research >Skin malformations in a neonatal foal tested homozygous positive for Warmblood Fragile Foal Syndrome
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Skin malformations in a neonatal foal tested homozygous positive for Warmblood Fragile Foal Syndrome

机译:新生儿小马驹的皮肤畸形经测试纯合为Warmblood易碎小马驹综合症阳性

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Background Skin malformations that resembled manifestations of Ehlers-Danlos-Syndrome were described in a variety of domestic animals during the last century as cutis hyperelastica, hyperelastosis cutis, dermatosparaxis, dermal/collagen dysplasia, dermal/cutaneous asthenia or Ehlers-Danlos-like syndrome/s. In 2007, the mutation responsible for Hereditary Equine Regional Dermal Asthenia (HERDA) in Quarter Horses was discovered. Several case reports are available for similar malformations in other breeds than Quarter Horses (Draught Horses, Arabians, and Thoroughbreds) including four case reports for Warmblood horses. Since 2013, a genetic test for the Warmblood Fragile Foal Syndrome Type 1 (WFFS), interrogating the causative point mutation in the equine procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 (PLOD1, or lysyl hydroxylase 1) gene, has become available. Only limited data are available on the occurrence rate and clinical characteristics of this newly detected genetic disease in horses. In humans mutations in this gene are associated with Ehlers-Danlos Syndrome Type VI (kyphoscoliotic form). Case presentation This is the first report describing the clinical and histopathological findings in a foal confirmed to be homozygous positive for WFFS. The Warmblood filly was born with very thin, friable skin, skin lesions on the legs and the head, and an open abdomen. These abnormalities required euthanasia just after delivery. Histologic examination revealed abnormally thin dermis, markedly reduced amounts of dermal collagen bundles, with loosely orientation and abnormally large spaces between deep dermal fibers. Conclusion WFFS is a novel genetic disease in horses and should be considered in cases of abortion, stillbirth, skin lesions and malformations of the skin in neonatal foals. Genetic testing of suspicious cases will contribute to evaluate the frequency of occurrence of clinical WFFS cases and its relevance for the horse population.
机译:背景上个世纪在各种家畜中描述了类似于埃勒斯-丹洛斯综合症表现形式的皮肤畸形,包括高弹性角质层,皮肤高弹性角质层,皮肤稀疏症,皮肤/胶原蛋白增生,皮肤/皮肤虚弱或埃勒斯-丹洛斯综合征/ s。在2007年,发现了导致四分之一匹马遗传性马区域性皮肤虚弱(HERDA)的突变。除四分之一匹(杂种马,阿拉伯人和纯种马)以外,其他品种中也有一些类似畸形的病例报告,其中包括四匹温布马的病例报告。自2013年以来,已对1种Warmblood脆弱小马驹综合症(WFFS)进行了基因测试,询问马前胶原蛋白赖氨酸,2-氧戊二酸5-二加氧酶1(PLOD1或赖氨酰羟化酶1)基因的致病点突变。 。关于这种新发现的马匹遗传病的发生率和临床特征,只有有限的数据。在人类中,该基因的突变与Ehlers-Danlos综合征VI型(脊柱后凸形式)有关。病例报告这是第一份报告,描述了证实为WFFS纯合子阳性的小马驹的临床和组织病理学发现。 Warmblood雌马出生时的皮肤非常脆弱,非常脆弱,腿和头部的皮肤都有损伤,腹部也很开放。这些异常在分娩后需要安乐死。组织学检查显示真皮层异常薄,真皮胶原束的数量明显减少,方向松散,真皮深层纤维之间的间隙异常大。结论WFFS是马的一种新型遗传病,应在流产,死胎,皮肤病灶和新生儿小马驹皮肤畸形的情况下予以考虑。对可疑病例进行基因检测将有助于评估临床WFFS病例的发生频率及其与马群的相关性。

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