Related Experiment Videos
[Case report: (erythro)keratoderma variabilis in a newborn foal].
1Klinik für Geburtshilfe, Gynäkologie und Andrologie der Gross- und Kleintiere mit Tierärztlicher Ambulanz, Justus-Liebig-Universität Giessen.
Berliner Und Munchener Tierarztliche Wochenschrift
|February 28, 2001
Summary
A rare congenital (Erythro)keratoderma variabilis case in a newborn foal is detailed. This study presents the clinical and histological findings of this equine skin condition.
Area of Science:
- Veterinary Dermatology
- Equine Pathology
Background:
- Congenital (Erythro)keratoderma variabilis is a rare inherited skin disorder.
- Keratodermas present as abnormal thickening of the skin, particularly the stratum corneum.
Observation:
- A newborn foal presented with generalized, symmetrical hyperkeratosis and erythema.
- Lesions were observed on the muzzle, ears, coronary bands, and soles of the feet.
Findings:
- Clinical examination revealed marked thickening and fissuring of the skin.
- Histopathological examination confirmed hyperkeratosis, acanthosis, and parakeratosis, consistent with (Erythro)keratoderma variabilis.
Implications:
- This case highlights the clinical presentation and diagnostic features of congenital (Erythro)keratoderma variabilis in foals.
- Understanding these findings aids in the diagnosis and management of inherited skin disorders in young horses.