Literature DB >> 18424829

The clinical and morphologic features of nonepidermolytic ichthyosis in the golden retriever.

E A Mauldin1, K M Credille, R W Dunstan, M L Casal.   

Abstract

A scaling disorder specific to Golden Retriever dogs has been recognized by both dermatologists and pathologists, but to date has not been well characterized. At the University of Pennsylvania's Laboratory of Toxicology and Pathology, 46 cases of ichthyosis were diagnosed histologically in Golden Retriever dogs from January 2004 to January 2007. A total of 22 dogs had skin lesions documented at younger than 1 year of age; 3 dogs between 1 and 2 years of age; 13 dogs developed lesions at older than 2 years; and the time of onset was unknown for 8 dogs. A total of 25 dogs were female, and 21 were male. All dogs had strikingly similar histopathologic changes that consisted of mild to moderate laminar orthokeratotic hyperkeratosis with an absence of epidermal hyperplasia and dermal inflammation. Ultrastructural analysis using a ruthenium tetroxide fixation method was performed on punch biopsy samples from 5 dogs and compared with 2 control dogs (1 clinically and histologically normal sibling of an affected dog and 1 Cairn Terrier). All affected dogs had retained and convoluted membranes with crystalline structures in the stratum corneum. Scattered keratinocytes in the granular cell layer had prominent, clear, membrane-bound, cytoplasmic vacuoles. Pedigree analysis of 14 dogs was compatible with autosomal recessive inheritance, but incomplete dominance could not be ruled out. This unique hyperkeratotic/scaling disorder in Golden Retrievers has distinctive clinical, histologic, and ultrastructural features, which are consistent with a primary cornification defect.

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Mesh:

Year:  2008        PMID: 18424829      PMCID: PMC3334879          DOI: 10.1354/vp.45-2-174

Source DB:  PubMed          Journal:  Vet Pathol        ISSN: 0300-9858            Impact factor:   2.221


  19 in total

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5.  Epidermolytic ichthyosis in a dog: clinical, histopathological, immunohistochemical and ultrastructural findings.

Authors:  L Mecklenburg; U Hetzel; S Ueberschär
Journal:  J Comp Pathol       Date:  2000-05       Impact factor: 1.311

6.  DNA sequence and physical mapping of the canine transglutaminase 1 gene.

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9.  Inability of keratinocytes lacking their specific transglutaminase to form cross-linked envelopes: absence of envelopes as a simple diagnostic test for lamellar ichthyosis.

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Authors:  K M Credille; K F Barnhart; J S Minor; R W Dunstan
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  10 in total

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3.  Autosomal Recessive Congenital Ichthyosis in American Bulldogs Is Associated With NIPAL4 (ICHTHYIN) Deficiency.

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4.  ABHD5 frameshift deletion in Golden Retrievers with ichthyosis.

Authors:  Sarah Kiener; Dominique J Wiener; Kaitlin Hopke; Alison B Diesel; Vidhya Jagannathan; Elizabeth A Mauldin; Margret L Casal; Tosso Leeb
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5.  A Defect in NIPAL4 Is Associated with Autosomal Recessive Congenital Ichthyosis in American Bulldogs.

Authors:  Margret L Casal; Ping Wang; Elizabeth A Mauldin; Gloria Lin; Paula S Henthorn
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6.  Prevalence of PNPLA1 Gene Mutation in 48 Breeding Golden Retriever Dogs.

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Review 7.  Inheritance of Monogenic Hereditary Skin Disease and Related Canine Breeds.

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8.  A de novo variant in the keratin 1 gene (KRT1) in a Chinese shar-pei dog with severe congenital cornification disorder and non-epidermolytic ichthyosis.

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Journal:  PLoS One       Date:  2022-10-17       Impact factor: 3.752

9.  PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans.

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10.  Isotretinoin Treatment for Autosomal Recessive Congenital Ichthyosis in a Golden Retriever.

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  10 in total

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