Peer-reviewed veterinary case report
Neonatal Coton de Tulear puppies with severe balance and movement
By Coates, Joan R et al.·Published in Journal of veterinary internal medicine·2002·Department of Veterinary Small Animal Medicine and Surgery, United States·View original on PubMed →
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Original publication title: Neonatal cerebellar ataxia in Coton de Tulear dogs.
- Species:
- dog
Plain-English summary
A group of Coton de Tulear puppies showed signs of severe coordination problems, including difficulty walking and standing, starting around 2 weeks of age. They had normal mental status but exhibited head shaking, tremors, and an unusual "swimming" motion when trying to move. Despite extensive testing, including brain scans and blood work, no specific cause was found, but the condition appeared to be stable and non-progressive for at least four months. It is suspected that this issue may be linked to a genetic trait affecting the development of the cerebellum, the part of the brain that controls movement.
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Abstract
A neonatal ataxia syndrome was observed in Coton de Tulear dogs. Seven affected pups (32%; 7/22) of both genders came from 5 different litters with phenotypically normal parents. Neurologic examination revealed normal mental status, head titubation, intention tremors, and severe gait, stance, and ocular ataxia beginning at 2 weeks of age. One of the pups was able to walk with assistance, but most of the affected pups were unable to stand and used propulsive movements ("swimming") for goal-oriented activities. They frequently would fall to lateral recumbency with subsequent decerebellate posturing and paddling. Ocular motor abnormalities included fine vertical tremors at rest and saccadic dysmetria. The condition was nonprogressive at least until 4 months of age. No specific abnormalities were identified in routine laboratory screening of blood and urine. Cerebrospinal fluid (CSF) analysis was normal in 1 dog, and a mild increase in protein concentration was observed in a second dog. CSF organic and amino acid concentrations were within normal limits. Magnetic resonance imaging and computed tomography of the brain, electromyography, motor nerve conduction studies, and brain stem auditory-evoked potentials were within normal limits. Postmortem examinations were performed on 5 affected dogs between 2 and 4 months of age. Routine light microscopic and immunocytochemical examination of brain, spinal cord, peripheral nerve, and muscle did not disclose any gross or histologic lesions. Compared with the cerebellum from an age-matched normal dog, the cerebellum from an affected dog showed synaptic abnormalities, including loss of presynaptic terminals and organelles associated with parallel fiber varicosities within the molecular layer and increased numbers of lamellar bodies in Purkinje cells. An autosomal recessive trait affecting development of the cerebellum is suspected.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/12465765/