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Myelomalacia is a pathological term referring to the softening of the spinal cord. [1] Possible causes of myelomalacia include cervical myelopathy , hemorrhagic infarction , or acute injury, such as that caused by intervertebral disc extrusion.
Cats with the homozygous genotype (MM) die before birth, and stillborn kittens show gross abnormalities of the central nervous system. [3] Cats with the heterozygous genotype (Mm) show severely shortened tail length, ranging from taillessness to a partial, stumpy tail. [3] Some Manx cats die before 12 months old and exhibit skeletal and organ ...
Clinical signs will generally present themselves in brief episodes of one to two minutes. [1] After such episode, the cat will generally return to its normal behaviour. [4] [5] These episodes can occur multiple times per day or per week, and may be triggered by endogenous or exogenous stimuli. [5]
This cyst, called a syrinx, can expand and elongate over time, destroying the spinal cord. The damage may result in loss of feeling, paralysis, weakness, [4] and stiffness in the back, shoulders, and extremities. Syringomyelia may also cause a loss of the ability to feel extremes of hot or cold, especially in the hands.
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Depending on climate and time zone, between the hours of 10:00 am to 4:00 pm, it is recommended to keep domesticated cats indoors, as the sun is at its highest peak between these times. Sun block is also available for cats, which can help prevent skin irritation, and a veterinarian should be contacted to find out which brands are appropriate ...
Cerebrospinal fluid fills the syrinx. Pressure differences along the spine cause the fluid to move within the cyst. Physicians believe that it is this continual movement of fluid that results in cyst growth and further damage to the spinal cord. In the case of syringomyelia, the syrinx can expand and elongate over time, destroying the spinal ...
In some breeds of cats, congenital sensorineural deafness is very common, with most white cats (but not albinos) being affected, particularly if they also have blue eyes. [1] The gene responsible for this defect is the KIT gene , and the disease is studied in the hope that it may shed light on the causes of hereditary deafness in humans. [ 8 ]