Hereditary xanthinuria in a goat
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- DOI 10.1111/jvim.15431
- PMID https://pubmed.ncbi.nlm.nih.gov/30758870
- PMCID https://www.ncbi.nlm.nih.gov/pmc/articles/6430956
- OpenAlex ID W2912724501
- Type Article
- Language EN
- Published 13 Feb 2019
- Volume 33 (2)
- Pages 1009–1014
- Source Journal of Veterinary Internal Medicine
- Publisher Wiley
- FWCI 0.35
- Countries 1
- Institutions 2
- Added 21 Feb 2019
- Updated 28 Oct 2026
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Hereditary xanthinuria in a goat
Article 2019 EN Gold
A 2-year-old mixed breed goat was presented for a 1-day history of anorexia and 1 week of weight loss. Serum biochemistry disclosed severe azotemia. Abdominal ultrasound examination showed decreased renal corticomedullary distinction, poor visualization of the renal pelves, and dilated ureters. On necropsy, the kidneys were small, the pelves were dilated, and the medulla was partially effaced by v…
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1 SDGsAuthors & Affiliations
7 authors| # | Author | Institutions | ORCID |
|---|---|---|---|
| 1 | Krystal J. Vail | Texas A&M University (US) | |
| 2 | Nicole M. Tate | University of Minnesota (US) | |
| 3 | Tasha Likavec | Texas A&M University (US) | — |
| 4 | Katie M. Minor | University of Minnesota (US) | |
| 5 | Philippa M. Gibbons | Texas A&M University (US) | |
| 6 | Raquel Rubia Rech | Texas A&M University (US) | |
| 7 | Eva Furrow Corresponding | University of Minnesota (US) |
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