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Schweizer Archiv fur Tierheilkunde1984; 126(11); 589-596;

[Dermatosparaxis in a foal and a cow–a rare disease?].

Abstract: No abstract available
Publication Date: 1984-11-01 PubMed ID: 6515392
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Cite This Article

APA
Witzig P, Suter M, Wild P, Rao VH, Steinmann B, von Rotz A. (1984). [Dermatosparaxis in a foal and a cow–a rare disease?]. Schweiz Arch Tierheilkd, 126(11), 589-596.

Publication

ISSN: 0036-7281
NlmUniqueID: 0424247
Country: Switzerland
Language: ger
Volume: 126
Issue: 11
Pages: 589-596

Researcher Affiliations

Witzig, P
    Suter, M
      Wild, P
        Rao, V H
          Steinmann, B
            von Rotz, A

              MeSH Terms

              • Animals
              • Cattle
              • Cattle Diseases / genetics
              • Cattle Diseases / pathology
              • Collagen
              • Female
              • Horse Diseases / genetics
              • Horse Diseases / pathology
              • Horses
              • Male
              • Skin / pathology
              • Skin Diseases / genetics
              • Skin Diseases / pathology
              • Skin Diseases / veterinary
              • Switzerland

              Citations

              This article has been cited 4 times.
              1. Rowe Á, Flanagan S, Barry G, Katz LM, Lane EA, Duggan V. Warmblood fragile foal syndrome causative single nucleotide polymorphism frequency in horses in Ireland. Ir Vet J 2021 Oct 18;74(1):27.
                doi: 10.1186/s13620-021-00206-1pubmed: 34663462google scholar: lookup
              2. Reiter S, Wallner B, Brem G, Haring E, Hoelzle L, Stefaniuk-Szmukier M, Długosz B, Piórkowska K, Ropka-Molik K, Malvick J, Penedo MCT, Bellone RR. Distribution of the Warmblood Fragile Foal Syndrome Type 1 Mutation (PLOD1 c.2032G>A) in Different Horse Breeds from Europe and the United States. Genes (Basel) 2020 Dec 18;11(12).
                doi: 10.3390/genes11121518pubmed: 33353040google scholar: lookup
              3. Bellone RR, Ocampo NR, Hughes SS, Le V, Arthur R, Finno CJ, Penedo MCT. Warmblood fragile foal syndrome type 1 mutation (PLOD1 c.2032G>A) is not associated with catastrophic breakdown and has a low allele frequency in the Thoroughbred breed. Equine Vet J 2020 May;52(3):411-414.
                doi: 10.1111/evj.13182pubmed: 31502696google scholar: lookup
              4. Monthoux C, de Brot S, Jackson M, Bleul U, Walter J. Skin malformations in a neonatal foal tested homozygous positive for Warmblood Fragile Foal Syndrome. BMC Vet Res 2015 Jan 31;11:12.
                doi: 10.1186/s12917-015-0318-8pubmed: 25637337google scholar: lookup