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The Veterinary record2001; 149(7); 199-203; doi: 10.1136/vr.149.7.199

Renal hypoplasia and dysplasia in an American miniature foal.

Abstract: Diagnostic imaging, including computed tomography, of a two-month-old foal with renal failure indicated that its right kidney was probably absent and that its left kidney was abnormal in shape. The foal was stabilised and released, but three days later its clinical signs recurred. Postmortem examination revealed renal hypoplasia and dysplasia, the first reported case of this condition in an American miniature horse.
Publication Date: 2001-09-11 PubMed ID: 11548957DOI: 10.1136/vr.149.7.199Google Scholar: Lookup
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Summary

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The research article discusses a case of a two-month-old foal examined for renal failure, where findings revealed an absence of the right kidney and an abnormal left kidney. Postmortem examination later showed presence of renal hypoplasia and dysplasia, marking the first reported occurrence of these conditions in an American miniature horse.

Details of the Case and Diagnostic Approach

  • The research revolves around a two-month-old American miniature foal. The foal was subjected to diagnostic imaging protocols due to symptoms indicative of renal failure.
  • Several techniques, including computed tomography (an imaging technique using computer-processed combinations of X-ray images), were used for thorough investigation.
  • This array of diagnostic imaging tests provided visual evidence suggesting the absence of the right kidney and abnormalities in the shape of the left kidney.

Post-Diagnostic Care and Postmortem Findings

  • After the diagnosis, the young horse underwent a stabilization procedure before being released. However, after three days, the foal’s previously observed signs resurfaced.
  • After its death, a postmortem examination was carried out. This examination provided insights into the internal conditions of the foal.
  • The postmortem findings revealed renal hypoplasia and dysplasia. Renal hypoplasia is a congenital condition characterized by an abnormally small kidney due to fewer than normal nephrons (the functional units of a kidney). On the other hand, renal dysplasia is a disordered development of kidneys resulting in abnormal kidney structure.

Significance of the Findings and Scope for Future Research

  • The findings from this case study are of particular significance as it represents the first reported instance of renal hypoplasia and dysplasia in an American miniature horse. These findings can contribute to the understanding of renal diseases in horses, in particular, and veterinary science, in general.
  • While single animal case studies provide limited data, they can form the basis for further research, spurring more extensive investigations into kidney diseases among the broader population of miniature horses.

Cite This Article

APA
Gull T, Schmitz DG, Bahr A, Read WK, Walker M. (2001). Renal hypoplasia and dysplasia in an American miniature foal. Vet Rec, 149(7), 199-203. https://doi.org/10.1136/vr.149.7.199

Publication

ISSN: 0042-4900
NlmUniqueID: 0031164
Country: England
Language: English
Volume: 149
Issue: 7
Pages: 199-203

Researcher Affiliations

Gull, T
  • Department of Large Animal Medicine and Surgery, College of Veterinary Medicine, Texas A&M University, College Station 77843-4475, USA.
Schmitz, D G
    Bahr, A
      Read, W K
        Walker, M

          MeSH Terms

          • Animals
          • Fatal Outcome
          • Female
          • Horse Diseases / diagnosis
          • Horse Diseases / pathology
          • Horses
          • Kidney / abnormalities
          • Kidney Diseases / pathology
          • Kidney Diseases / veterinary
          • Renal Insufficiency / etiology
          • Renal Insufficiency / veterinary
          • Tomography, X-Ray Computed

          Citations

          This article has been cited 1 times.
          1. Medina-Torres CE, Hewson J, Stämpfli S, Stalker MJ. Bilateral diffuse cystic renal dysplasia in a 9-day-old Thoroughbred filly.. Can Vet J 2014 Feb;55(2):141-6.
            pubmed: 24489392