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Tierarztliche Praxis1994; 22(3); 252-255;

[The “lethal white foal” syndrome].

Abstract: The lethal white foal syndrome (congenital intestinal aganglionosis) was diagnosed by history, clinical signs and pathological findings in a female foal, born in March 1992, that was an offspring of two overo-spotted paint horses. The syndrome is a congenital innervation defect of the gastrointestinal tract. A literature review of this condition, relatively unknown in Germany, is given.
Publication Date: 1994-06-01 PubMed ID: 8048034
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Summary

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The research article deals with the lethal white foal syndrome, a rare genetic disorder in foals, using a case study of a female foal born in March 1992. This syndrome is characterized by a congenital defect in innervation of the gastrointestinal tract.

Introduction and Case Study

The article revolves around the case study of lethal white foal syndrome (also known as congenital intestinal aganglionosis). The term “aganglionosis” refers to a situation where ganglions, the body’s nerve cell clusters, are absent in certain parts of the body, causing significant health issues. In this particular case, the foal, which is an offspring of two overo-spotted paint horses, is unable to properly digest food due to the absence of certain nerve cells in the gastrointestinal tract.

Overview of Lethal White Foal Syndrome

  • Lethal white foal syndrome is a condition primarily found in horses where the foal is born with an underdeveloped or completely non-existent gastrointestinal system.
  • Due to the lack of a properly functioning digestive system, the afflicted foal faces malnutrition and related health issues, eventually leading to death, hence the term “lethal”.
  • It’s a congenital condition, meaning it’s present at birth and is often the result of the offspring’s parents having the overo color pattern. In particular, when both parents have this color pattern, it seems to increase the likelihood of the condition occurring in their offspring.

Importance and Relevance of the Study

The study undertakes an exploration of this relatively unknown condition in Germany. While the condition is known, it seems there may be a lack of comprehensive knowledge or awareness in this region, making detailed study important in enhancing understanding and potentially improving preventive strategies or treatments, if available. The article, through the case study, diagnosis, and literary review aims to shed light on this fatal condition.

Conclusion

The study through its examination of the case of a female foal born in March 1992, provides a comprehensive understanding of the lethal white foal syndrome. The syndrome, marked by a congenital innervation defect in the gastrointestinal tract, has been analyzed in the framework of history, clinical signs, and pathological findings. The findings drawn from this study play a significant role in enriching the understanding of this condition, especially in regions where knowledge about it is relatively scarce.

Cite This Article

APA
Blendinger C, Müller G, Bostedt H. (1994). [The “lethal white foal” syndrome]. Tierarztl Prax, 22(3), 252-255.

Publication

ISSN: 0303-6286
NlmUniqueID: 7501042
Country: Germany
Language: ger
Volume: 22
Issue: 3
Pages: 252-255

Researcher Affiliations

Blendinger, C
  • Ambulatorischen und Geburtshilflichen Veterinärklinik, Justus-Liebig-Universität Giessen.
Müller, G
    Bostedt, H

      MeSH Terms

      • Animals
      • Female
      • Hirschsprung Disease / pathology
      • Hirschsprung Disease / veterinary
      • Horse Diseases / congenital
      • Horse Diseases / pathology
      • Horses
      • Piebaldism / pathology
      • Piebaldism / veterinary
      • Syndrome

      Citations

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