Literature DB >> 1155959

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

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

Abstract

Ultrastructural examination was performed in 8 biopsies from 4 patients with the Pasini type of epidermolysis bullosa dystrophica dominans. The biopsies were taken from: 1. clinically normal skin from nonpredilection areas, 2. intact skin from predilection areas, 3. involved skin and 4. experimentally frictioned skin. The main ultrastructural alterations detected are as follows: hypoplasia of anchoring fibrils, split or blister formation between basal lamina and dermis, hernia-like protrusion of basal cells, sub- and intraepidermal deposition of fibrillar bodies, and duplications of basal lamina. Among them, the constantly observed finding in all of the four biopsy groups in the structural defect of anchoring fibrils, namely, that the anchoring fibrils are rudimentary and reduced in number. Presence of the structural defect of anchoring fibrils in clinically normal skin from nonpredilection areas in patients with the Pasini type of epidermolysis bullosa dystrophica dominans indicates that this defect is not a secondary change following repeated mechanical trauma, but a primary, genetically determined event.

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Year:  1975        PMID: 1155959

Source DB:  PubMed          Journal:  Arch Dermatol Forsch        ISSN: 0003-9187


  23 in total

1.  Electron microscope studies of dermal-epidermal separation in human skin.

Authors:  R W PEARSON; B SPARGO
Journal:  J Invest Dermatol       Date:  1961-03       Impact factor: 8.551

2.  Ultrastructure of inborn errors of keratinization. VI. Inherited ichthyoses--a model system for heterogeneities in keratinization disturbances.

Authors:  I Anton-Lamprecht; U W Schnyder
Journal:  Arch Dermatol Forsch       Date:  1974

3.  [Origin and nature of fibrillar bodies (author's transl)].

Authors:  I Anton-Lamprecht; W Tilgen
Journal:  Arch Dermatol Forsch       Date:  1973-05-28

4.  Histochemistry and fine structure of oral lesions of mucous membrane pemphigoid. Preliminary observations.

Authors:  F R Susi; G Shklar
Journal:  Arch Dermatol       Date:  1971-09

5.  Light and electron microscopic studies of physical injury to the skin. II. Friction.

Authors:  J A Hunter; E McVittie; J S Comaish
Journal:  Br J Dermatol       Date:  1974-05       Impact factor: 9.302

6.  Dermal and epidermal types of erythema multiforme. A histopathologic study of 24 cases.

Authors:  C E Orfanos; G Schaumburg-Lever; W F Lever
Journal:  Arch Dermatol       Date:  1974-05

7.  Ultrastructural aspects of dermatitis herpetiformis (Duhring's disease).

Authors:  F G Rodrigo
Journal:  Br J Dermatol       Date:  1972-04       Impact factor: 9.302

8.  [Ultrastructure of inborn erors of keratinization. I. Ichthyosis congenita].

Authors:  I Anton-Lamprecht
Journal:  Arch Dermatol Forsch       Date:  1972

9.  [Fine structure investigations in hereditary recessive dystrophic epidermolysis bullosa].

Authors:  A Vogel; U W Schnyder
Journal:  Dermatologica       Date:  1967

10.  Inherited disorders of the skin and skin diseases due to a hereditary predisposition.

Authors:  U W Schnyder
Journal:  J Dermatol       Date:  1974-09       Impact factor: 4.005

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  11 in total

1.  Epidermolysis bullosa dystorphica and systemic lupus erythematosus.

Authors:  G C Archibald
Journal:  Proc R Soc Med       Date:  1976-12

2.  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

3.  Pathology of collagen degradation. A review.

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

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

Authors:  I Hashimoto; T Gedde-Dahl; U W Schnyder; I Anton-Lamprecht
Journal:  Arch Dermatol Res       Date:  1976-06-21       Impact factor: 3.017

5.  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

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

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

7.  Prenatal diagnosis of genetic disorders of the skin by means of electron microscopy.

Authors:  I Anton-Lamprecht
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

8.  Ultrastructural studies in epidermolysis bullosa hereditaria. IV. Recessive dystrophic types with junctional blistering. (Infantile or Herlitz-Pearson type and adult type).

Authors:  I Hashimoto; T Gedde-Dahl; U W Schnyder; I Anton-Lamprecht
Journal:  Arch Dermatol Res       Date:  1976-11-26       Impact factor: 3.017

9.  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

10.  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

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