SavedAdd your journal

Journals / Kocatepe Veteriner Dergisi / 2018 / Cilt: 11 - Sayı: 3

Vitamin D Levels in Cat and Dogs With Ehlers-Danlos Syndrome: Case Series Touching Nutritional Deficiency Hypothesis

Ehlers-Danlos Sendromlu Kedi ve Köpeklerde D Vitamini Düzeyleri: Nutrisyonel Bozukluk Hipotezine Dair Olgu Serisi

Hasan ERDOĞAN
Kerem URAL
Deniz Sude ATEŞ
Pelin KANDEMİR
Pages
339–343
Publication Date
2018-09-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Just as dog and cats diagnosed with EDS found lower vitamin D levels (total 8 of 10) are considered, it has recommended in cat and dogs with EDS taking into account of vitamin D deficiency as well as some other nutritional deficiencies and giving oral vitamin D supplements with safety as human medicine.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Ehlers Danlos syndrome (EDS) reported varied animal species is a rare hereditary collagen disorder standing out reduced strength of skin being hyperextensible, velvety and fragile.
📊
Key Findings & Data:Diagnosis of also termed dermatosparaxis or cutaneous asthenia in animals is based on classic clinical symptoms, skin extensibility index with histopathologic examination included thin, unregular seperated collagen bundles.
💡
Conclusion & Impact:Just as dog and cats diagnosed with EDS found lower vitamin D levels (total 8 of 10) are considered, it has recommended in cat and dogs with EDS taking into account of vitamin D deficiency as well as some other nutritional deficiencies and giving oral vitamin D supplements with safety as human medicine.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Ehlers-Danlos Sendromu · kedi · köpek

Abstract

Ehlers Danlos syndrome (EDS) reported varied animal species is a rare hereditary collagen disorder standing out reduced strength of skin being hyperextensible, velvety and fragile. Diagnosis of also termed dermatosparaxis or cutaneous asthenia in animals is based on classic clinical symptoms, skin extensibility index with histopathologic examination included thin, unregular seperated collagen bundles. In the presented case series enrolled different ages (1-3 years old 4 cats; and 1-5 years old 6 dogs) with both gender cats (2 males, 2 females) and dogs (4 males, 2 females) has been conferred serum 25 (OH) D3 levels associations. Just as dog and cats diagnosed with EDS found lower vitamin D levels (total 8 of 10) are considered, it has recommended in cat and dogs with EDS taking into account of vitamin D deficiency as well as some other nutritional deficiencies and giving oral vitamin D supplements with safety as human medicine.

Özet

Farklı hayvan türlerinde bildirilen ve derinin elastikiyetinde azalma, deride aşırı uzama, yumuşama bulgular gösteren Ehlers Danlos Sendromu (EDS) nadir görülen kalıtsal kollojen hastalığıdır. Hayvanlarda dermatosparaksis ve kutanöz astenia olarak da bilinen bu hastalığın tanısı klasik klinik bulgular, cilt uzayabilirlik indeksi ile histopatolojide kalın, düzensiz ayrılmış kollojen demetlerinin görülmesine dayanmaktadır. Farklı yaş (n=4 kedi; 1-3 yaşlı ile n=6 köpek 1-5 yaşlı), her 2 cinsiyetten kedi (2 erkek, 2 dişi) ve köpeğin (4 erkek, 2 dişi) dahil edildiği olgu serisinde serum 25 (OH) D3 seviyeleri ile ilişkileri sunulmaktadır. EDS tanısı konulan kedi ve köpeklerde bulunan düşük vitamin D seviyeleri (toplamda 8/10) düşünüldüğünde EDS’ li kedi ve köpeklerde diğer beslenme eksikliklerinin yanı sıra vitamin D yetersizliğinin de göz önüne alınması gerektiği ve beşeri hekimlikte olduğu gibi oral vitamin D takviyesinin güvenle verilebileceği önerilmektedir.

🔖

Cite This Article

ERDOĞAN, H., URAL, K., ATEŞ, D. S., KANDEMİR, P. (2018). Vitamin D Levels in Cat and Dogs With Ehlers-Danlos Syndrome: Case Series Touching Nutritional Deficiency Hypothesis. Kocatepe Veteriner Dergisi, Cilt: 11 - Sayı: 3, 339–343. https://ajindex.com/articles/124793

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (13)

  1. Pyeritz RE. Ehlers-Danlos syndrome. N Engl J Med. 2000; 342(10):730–2.
  2. De Paepe A, Malfait F. The Ehlers-Danlos syndrome, a disorder with many faces. Clin Genet. 2012; 82(1):1–11.
  3. Beighton P, De Paepe A, Steinmann B, Tsipouras P, Wenstrup RJ. Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK). Am J Med Genet. 1998; 77(1):31–7. Beighton P, de Paepe A, Danks D, Finidori G, Gedde-Dahl T, Goodman R, Hall JG, Hollister DW, Horton W, McKusick VA, et al. International nosology of heritable disorders of connective tissue, Berlin, 1986. Am J Med Genet.1988; 29(3):581–94. Germain DP. Ehlers-Danlos syndrome type IV. Orphanet J Rare Dis. 2007; 2:32. De Felice C, Bianciardi G, Dileo L, Latini G, Parrini S. Abnormal oral vascular network geometric complexity in Ehlers-Danlos syndrome. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2004; 98(4):429–34.
  4. Lum YW, Brooke BS, Black 3rd JH. Contemporary management of vascular Ehlers-Danlos syndrome. Curr Opin Cardiol. 2011; 26(6):494–501.
  5. Oderich GS, Panneton JM, Bower TC, Lindor NM, Cherry KJ, Noel AA, Kalra M, Sullivan T, Gloviczki P. The spectrum, management and clinical outcome of Ehlers-Danlos syndrome type IV: a 30-year experience. J Vasc Surg. 2005; 42(1):98–106.
  6. Pepin M, Schwarze U, Superti-Furga A, Byers PH. Clinical and genetic features of Ehlers-Danlos syndrome type IV, the vascular type. N Engl J Med. 2000; 342(10):673–80.
  7. Bergqvist D, Bjorck M, Wanhainen A. Treatment of vascular Ehlers-Danlos syndrome: a systematic review. Ann Surg. 2013; 258(2):257–61.
  8. Busch A, Suellner J, Anger F, Meir M, Kickuth R, Lorenz U, Wildenauer R. Critical care of kyphoscoliotic type Ehlers-Danlos syndrome with recurrent vascular emergencies. VASA Zeitschrift fur Gefasskrankheiten. 2014; 43(3):216–21.
  9. Horowitz MB, Purdy PD, Valentine RJ, Morrill K. Remote vascular catastrophes after neurovascular interventional therapy for type 4 Ehlers-Danlos Syndrome. AJNR Am J Neuroradiol. 2000; 21(5):974–6.
  10. Malfait F, De Paepe A. Bleeding in the heritable connective tissue disorders: mechanisms, diagnosis and treatment. Blood Rev. 2009; 23(5):191–7.
  11. Asherson RA, Bosman C, Tikly M, Spiro F, Pope FM. Ehlers-Danlos syndrome type IV in a young man. J Rheumatol. 2006; 33(10):2091–6.
  12. Calatzis A, Heesen M, Heesen M, Spannagl M. [Point-of-care testing of hemostatic alterations in anaesthesia and intensive care]. Anaesthesist. 2003; 52(3):229–37.
  13. Lindsay H, Lee-Kim YJ,