Peer-reviewed veterinary case report
Puppy with brain and spinal cord damage from acid buildup
By Podell, M et al.·Published in Metabolic brain disease·1996·Department of Veterinary Clinical Sciences, United States·View original on PubMed →
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Original publication title: Methylmalonic and malonic aciduria in a dog with progressive encephalomyelopathy.
- Species:
- dog
Plain-English summary
A 12-week-old female Labrador retriever was brought in with worsening neurological symptoms, including issues with movement and coordination. After several months, tests revealed she had a metabolic disorder causing the buildup of certain acids in her body, which was linked to her brain and spinal cord degeneration. Unfortunately, despite the diagnosis, the condition is serious and progressive, and the dog’s symptoms were related to significant brain abnormalities. There is no specific treatment for this type of metabolic disorder, and the prognosis is poor due to the ongoing neurological decline.
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Abstract
A 12 week old female Labrador retriever dog with signs of progressive diffuse degeneration of the brain and spinal cord was found to have methylmalonic and malonic aciduria. Over a 5 month period, the dog developed neurologic signs compatible with disease of the central nervous system with predominant diffuse cerebral and right lateralizing brainstem deficits. Gross pathological examination of the brain showed that the lateral, third, and fourth ventricles of the brain were markedly enlarged and associated with white and grey matter atrophy. Syringomyelia and hydromyelia of the central canal into the dorsal funiculus of the spinal cord beginning at the level of the cervical intumescence and extending to the lumbar intumescence was also present. Significant biochemical abnormalities include methylmalonic and malonic aciduria, mild lactic and pyruvic aciduria. There was also accumulation of citric acid cycle intermediates including succinic, aconitic, and fumaric acids. Disordered fatty acid oxidation was suggested by increased excretion of adipic, ethylmalonic, suberic and sebacic acids. Neither ketoacidosis nor hyperammonemia were present, and serum cobalamin levels were normal. Overall, this dog demonstrates an inborn error of metabolism resulting in abnormal organic acid accumulation associated with a neurodegenerative disease.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/8869944/