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猫的畸形与曼岛综合征

Malformations and the Manx syndrome in cats.

作者信息

Deforest M E, Basrur P K

出版信息

Can Vet J. 1979 Nov;20(11):304-14.

Abstract

Breeding experiments were conducted on cats with congenital taillessness, to test the dissemination pattern of taillessness in their offspring. Clinical evaluation, radiographic analysis of the vertebral column and histological studies of the digestive tract and central nervous tissue were conducted to determine the association of malformations of these systems in cats born with different degrees of taillessness noted in the rumpy and stumpy cats. The mode of transmission of the tailless (Manx) condition assumed to be through an autosomal dominant factor (M) was confirmed by this investigation. It is hypothesized that the problems associated with the tailless condition such as spina bifida, urinary and faecal incontinence and locomotor disturbances of the pelvic limbs may all be related to a disturbance affecting the development of the central nervous system in the early embryonic life.

摘要

对患有先天性无尾症的猫进行了繁殖实验,以测试无尾症在其后代中的传播模式。进行了临床评估、脊柱的放射学分析以及消化道和中枢神经组织的组织学研究,以确定在臀部无尾和短尾猫中出生的不同程度无尾症的猫中这些系统畸形之间的关联。本研究证实了无尾(曼岛猫)性状的遗传方式假定是通过常染色体显性因子(M)。据推测,与无尾症相关的问题,如脊柱裂、大小便失禁和骨盆四肢的运动障碍,可能都与早期胚胎生命中影响中枢神经系统发育的干扰有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a21/1789620/5b6be9d514c5/canvetj00324-0023-a.jpg

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