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  2. Feline hyperesthesia syndrome - Wikipedia

    en.wikipedia.org/wiki/Feline_hyperesthesia_syndrome

    Information on a cat's tendency towards obsessive compulsive disorders, anxiety, fear, and over-attachment to its owner is highly advantageous for diagnosis and treatment. Wherever possible, cases of feline hyperesthesia syndrome should be referred to a specialist in feline behaviour for a secondary opinion.

  3. Feline spongiform encephalopathy - Wikipedia

    en.wikipedia.org/wiki/Feline_spongiform...

    Affected cats may also display poor judgement of distance, and some cats may develop a rapid, crouching, hypermetric gait. Some affected cats may exhibit an abnormal head tilt, tremors, a vacant stare, excessive salivation, decreased grooming behaviors, polyphagia , and dilated pupils. [ 3 ]

  4. SPATCCM - Wikipedia

    en.wikipedia.org/wiki/SPATCCM

    Treatment anti-epileptics Spastic tetraplegia, thin corpus callosum, and progressive microcephaly (often referred to by its acronym SPATCCM ) is a rare autosomal recessive disease caused by mutations in the SLC1A4 gene encoding the ASCT1 protein.

  5. MITSIE VARGAS: Chronic pain in cats can be hard to diagnose - AOL

    www.aol.com/news/mitsie-vargas-chronic-pain-cats...

    Conditions like bad teeth, interstitial cystitis, ulcers, dermatitis, diabetic neuropathy, pancreatitis, cancer, and IBD can create chronic pain. MITSIE VARGAS: Chronic pain in cats can be hard to ...

  6. Hypersomatotropism (veterinary) - Wikipedia

    en.wikipedia.org/wiki/Hypersomatotropism...

    Cats suffering from hypersomatotropism show a multitude of symptoms, the majority of these symptoms are not useful for identifying hypersomatotropism instead of just diabetes mellitus. The presence and level of severity of symptoms vary based on levels of growth hormone excess and duration of excess secretion.

  7. Cernunnos deficiency - Wikipedia

    en.wikipedia.org/wiki/Cernunnos_deficiency

    Treatment Immunoglobulin replacement, HSCT [ 1 ] Cernunnos deficiency is a form of combined immunodeficiency characterized by microcephaly , due to mutations in the NHEJ1 gene, it is inherited via autosomal recessive manner [ 2 ] [ 1 ] Management for this condition is antiviral prophylaxis and antibiotic treatment.