Literature DB >> 942257

Ultrastructural studies in epidermolysis bullosa hereditaria. II. Dominant dystrophic type of Cockayne and Touraine.

I Hashimoto, T Gedde-Dahl, U W Schnyder, I Anton-Lamprecht.   

Abstract

Ultrastructural examination was performed in 9 biopsy specimens from 4 patients with the Cockayne-Touraine type of epidermolysis bullosa dystrophica dominans. The specimens were taken from: 1. clinically normal skin from the blister-nonpredilected sites (trunk) as well as 2. atrophic, 3. intact, and 4. experimentally frictioned skin regions from the blister-predilected sites (extremities). In the frictioned skin a dermolytic blister formations was observed. Development of anchoring fibrils showed a marked regional difference, the counts of fibrils being significantly lower (40%) in the predilection sites than in the nonpredilection sites. In addition the anchoring fibrils showed a variable degree of abnormal structure. The low frequency of often abnormally structured anchoring fibrils in the blister-preferred sites provides a good explanation for the clinical features. More studies are needed to see if regional differences in fibril frequency is a feature also of normal skin, in which case the dominant epidermolysis gene may represent a mutated structural anchoring fibril gene.

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Year:  1976        PMID: 942257     DOI: 10.1007/bf00561499

Source DB:  PubMed          Journal:  Arch Dermatol Res            Impact factor:   3.017


  7 in total

1.  [ON THE CLINICAL PICTURE AND GENETICS OF DOMINANT DYSTROPHIC HEREDITARY EPIDERMOLYSIS BULLOSA].

Authors:  U W SCHNYDER; D EICHHOFF
Journal:  Arch Klin Exp Dermatol       Date:  1963-12-19

2.  [Ultrastructure of inborn errors of keratinization. 3. Autosomal dominant ichthyosis vulgaris (author's transl)].

Authors:  I Anton-Lamprecht
Journal:  Arch Dermatol Forsch       Date:  1973-12-05

3.  [Epidermolysis bullosa dystrophica dominans-a defect of the anchoring fibrils? (authors transl)].

Authors:  I Anton-Lamprecht; U W Schnyder
Journal:  Dermatologica       Date:  1973

4.  Epidermolysis bullosa dystrophica dominans (Pasini)-a primary structural defect of the anchoring fibrils.

Authors:  I Anton-Lamprecht; I Hashimoto
Journal:  Hum Genet       Date:  1976-04-15       Impact factor: 4.132

5.  Ultrastructural studies in epidermolysis bullosa heriditaria. I. Dominant dystrophic type of Pasini.

Authors:  I Hashimoto; I Anton-Lamprecht; T Gedde-Dahl; U W Schnyder
Journal:  Arch Dermatol Forsch       Date:  1975

6.  Epidermolysis bullosa dystrophica-recessive: a possible role of anchoring fibrils in the pathogenesis.

Authors:  R A Briggaman; C E Wheeler
Journal:  J Invest Dermatol       Date:  1975-08       Impact factor: 8.551

7.  Ultrastructural studies in epidermolysis bullosa hereditaria. III. Recessive dystrophic types with dermolytic blistering (Hallopeau-Siemens types and inverse type).

Authors:  I Hashimoto; U W Schnyder; I Anton-Lamprecht; T Gedde-Dahl; S Ward
Journal:  Arch Dermatol Res       Date:  1976-08-27       Impact factor: 3.017

  7 in total
  7 in total

1.  Compound heterozygosity for COL7A1 mutations in twins with dystrophic epidermolysis bullosa: a recessive paternal deletion/insertion mutation and a dominant negative maternal glycine substitution result in a severe phenotype.

Authors:  A M Christiano; I Anton-Lamprecht; S Amano; U Ebschner; R E Burgeson; J Uitto
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

2.  Pathology of collagen degradation. A review.

Authors:  R Pérez-Tamayo
Journal:  Am J Pathol       Date:  1978-08       Impact factor: 4.307

3.  Epidermolysis bullosa pruriginosa: A report of two cases.

Authors:  Varadraj Vasant Pai; Tukaram Sori; Kikkeri Narayanshetty Naveen; Sharatchandra Bhimrao Athanikar; Vijetha Rai; Dinesh Udupi Shastry
Journal:  Indian Dermatol Online J       Date:  2014-01

4.  Epidermolysis bullosa simplex generalisata: importance of immunofluorescence studies in early diagnosis.

Authors:  H Baker
Journal:  Arch Dermatol Res       Date:  1982       Impact factor: 3.017

5.  Chronic leg ulcers as a rare cause for the first diagnosis of epidermolysis bullosa dystrophica.

Authors:  Mazin G Bafaraj; Elvir Cesko; Maren Weindorf; Joachim Dissemond
Journal:  Int Wound J       Date:  2012-09-13       Impact factor: 3.315

6.  Ultrastructural studies in epidermolysis bullosa hereditaria. III. Recessive dystrophic types with dermolytic blistering (Hallopeau-Siemens types and inverse type).

Authors:  I Hashimoto; U W Schnyder; I Anton-Lamprecht; T Gedde-Dahl; S Ward
Journal:  Arch Dermatol Res       Date:  1976-08-27       Impact factor: 3.017

7.  Epidermolysis bullosa simplex: expression of gelatinase activity in cultured human skin fibroblasts.

Authors:  J O Winberg; T Gedde-Dahl
Journal:  Biochem Genet       Date:  1992-08       Impact factor: 1.890

  7 in total

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