Literature DB >> 17222238

Clinical and pathological findings in a HERDA-affected foal for 1.5 years of life.

Stephen D White1, Verena K Affolter, Patricia C Schultheiss, Barry A Ball, Myrthe T Wessel, Phillip Kass, Annette M Molinaro, Danika L Bannasch, Peter J Ihrke.   

Abstract

A Quarter horse filly bred from two horses affected with HERDA (hereditary equine regional dermal asthenia) was observed clinically and its skin histologically for the 1.5 years of its life. Severe signs of the disease did not manifest until 1.5 years of age, and were not temporally related to saddling. Histological comparison to an age-, breed- and sex-matched control did not show any consistent diagnostic features. Monitoring of the proband substantiated previous reports of (i) the autosomal recessive nature of the disease, (ii) mares affected with HERDA being able to foal without damage to the skin or reproductive tract, (iii) HERDA foals appearing phenotypically normal throughout the first year of life, and (iv) demonstrated that histological interpretation of skin specimens from grossly normal skin may be insufficient to differentiate HERDA-affected horses from controls.

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Year:  2007        PMID: 17222238     DOI: 10.1111/j.1365-3164.2007.00562.x

Source DB:  PubMed          Journal:  Vet Dermatol        ISSN: 0959-4493            Impact factor:   1.589


  3 in total

Review 1.  Equine clinical genomics: A clinician's primer.

Authors:  M M Brosnahan; S A Brooks; D F Antczak
Journal:  Equine Vet J       Date:  2010-10       Impact factor: 2.888

2.  Skin malformations in a neonatal foal tested homozygous positive for Warmblood Fragile Foal Syndrome.

Authors:  Chloé Monthoux; Simone de Brot; Michelle Jackson; Ulrich Bleul; Jasmin Walter
Journal:  BMC Vet Res       Date:  2015-01-31       Impact factor: 2.741

3.  Distribution of the Warmblood Fragile Foal Syndrome Type 1 Mutation (PLOD1 c.2032G>A) in Different Horse Breeds from Europe and the United States.

Authors:  Simone Reiter; Barbara Wallner; Gottfried Brem; Elisabeth Haring; Ludwig Hoelzle; Monika Stefaniuk-Szmukier; Bogusława Długosz; Katarzyna Piórkowska; Katarzyna Ropka-Molik; Julia Malvick; Maria Cecilia T Penedo; Rebecca R Bellone
Journal:  Genes (Basel)       Date:  2020-12-18       Impact factor: 4.096

  3 in total

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