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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为Warmblood易碎小马驹综合症阳性

摘要

BACKGROUND:ududSkin 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).ududCASE PRESENTATION:ududThis 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.ududCONCLUSION:ududWFFS 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:在上个世纪的许多家畜中,类似于Ehlers-Danlos综合征表现的皮肤畸形被描述为皮肤高弹性,皮肤弹性过高,皮肤晶状体剥脱,皮肤/胶原蛋白增生,皮肤/皮肤无力或Ehlers-Danlos样综合征。 2007年,发现了导致四分之一匹马遗传性马区域性皮肤虚弱症(HERDA)的突变。除四分之一匹(杂种马,阿拉伯人和纯血种马)以外,其他品种中也有一些类似畸形的病例报告,其中包括四匹温血马的病例报告。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-双加氧酶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遗传病在马中的发生率和临床特征,只有有限的数据。在人类中,此基因的突变与Ehlers-Danlos综合征VI型(后遗症)有关。 ud ud病情介绍: ud ud这是第一份报告,描述了小马驹的临床和组织病理学发现,证实该小马驹为WFFS纯合子阳性。 Warmblood雌马出生时的皮肤非常脆弱,非常脆弱,腿部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。 ud ud结论: ud udWFFS是马的一种新型遗传病,在以下情况下应考虑使用新生儿小马驹的流产,死产,皮肤病变和皮肤畸形。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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