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Peer-reviewed veterinary case report

Perosomus elumbis, cerebral aplasia, and spina bifida in an aborted thoroughbred foal.

Journal:
Research in veterinary science
Year:
2012
Authors:
Gerhauser, I et al.
Affiliation:
Department of Pathology · Germany
Species:
horse

Plain-English summary

This report discusses a rare condition called perosomus elumbis, which affects the spinal cord and vertebrae, in a Thoroughbred foal that was aborted. The foal had several serious issues, including problems with the brain and spine, as well as malformations in the urinary and intestinal systems. Tests did not find any signs of infection or specific viruses that could explain these abnormalities. The exact cause of these developmental problems is still unclear, but it might be related to genetic factors, exposure to harmful substances, or issues with the mare's metabolism during pregnancy. Unfortunately, the outcome was not successful, as the foal did not survive.

Abstract

Perosomus elumbis represents a rare congenital anomaly characterized by aplasia of the lumbosacral spinal cord and vertebrae. This anomaly is often associated with arthrogryposis and malformations of the urogenital and intestinal tract. This report describes the first case of perosomus elumbis in an aborted Thoroughbred foal associated with cerebral aplasia with meningocele, cranioschisis, spina bifida, a fused urogenital and intestinal tracts lined by a cutaneous mucosa without uterine glands, atresia ani, and arthrogryposis of the hind legs. Immunohistochemistry detected no abnormalities in the GFAP, S-100, vimentin, NeuN, doublecortin, and neurofilament expression pattern in the remnants of the brainstem. Pathogenic bacteria or equine herpesviruses one and four were not found using a microbiological investigation or polymerase chain reaction, respectively. The observed malformations may be induced by a severe developmental disturbance during the formation of the neural tube with secondary distortion of the surrounding mesoderm. Although the aetiology of this dysorganogenesis remains undetermined, inherited chromosomal mutations, an intake of different xenobiotics, and/or a disturbed metabolism of the mare may have caused the defect.

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Original publication: https://pubmed.ncbi.nlm.nih.gov/21146843/