Literature DB >> 3228192

A disease resembling junctional epidermolysis bullosa in a toy poodle.

R W Dunstan1, R C Sills, J E Wilkinson, A S Paller, K H Hashimoto.   

Abstract

A disease resembling junctional epidermolysis bullosa in humans is described in a toy poodle. Shortly after birth, the affected animal developed vesicles and bullae on the pads of the feet and the mucous membranes of the oral cavity. The lesions rapidly increased in number and severity, eventually involving the glabrous skin of the ventral abdomen. Due to the severity of the lesions, the animal was euthanized when it was 48 h old. Histopathologic, ultrastructural and immunohistochemical evaluation defined a minimally inflamed subepidermal vesicular disease with separation occurring at the zona lucida of the basement membrane zone. Laminin and type IV collagen were present at the base of the vesicle.

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Year:  1988        PMID: 3228192

Source DB:  PubMed          Journal:  Am J Dermatopathol        ISSN: 0193-1091            Impact factor:   1.533


  3 in total

1.  A mouse model of generalized non-Herlitz junctional epidermolysis bullosa.

Authors:  Jason A Bubier; Thomas J Sproule; Lydia M Alley; Cameron M Webb; Jo-David Fine; Derry C Roopenian; John P Sundberg
Journal:  J Invest Dermatol       Date:  2010-03-25       Impact factor: 8.551

2.  A frameshift mutation within LAMC2 is responsible for Herlitz type junctional epidermolysis bullosa (HJEB) in black headed mutton sheep.

Authors:  Stefanie Mömke; Andrea Kerkmann; Anne Wöhlke; Miriam Ostmeier; Marion Hewicker-Trautwein; Martin Ganter; James Kijas; Ottmar Distl
Journal:  PLoS One       Date:  2011-05-04       Impact factor: 3.240

3.  A COL7A1 Variant in a Litter of Neonatal Basset Hounds with Dystrophic Epidermolysis Bullosa.

Authors:  Teresa Maria Garcia; Sarah Kiener; Vidhya Jagannathan; Duncan S Russell; Tosso Leeb
Journal:  Genes (Basel)       Date:  2020-12-04       Impact factor: 4.096

  3 in total

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