Assuntos
Transtornos da Audição/genética , Transtornos da Pigmentação/genética , Transtornos da Visão/genética , Adulto , Animais , Doenças do Gato/embriologia , Gatos , Doenças do Cão/embriologia , Cães , Feminino , Transtornos da Audição/embriologia , Humanos , Transtornos da Pigmentação/embriologia , Transtornos da Visão/embriologia , Síndrome de Waardenburg/embriologiaRESUMO
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.
