Literature DB >> 1270327

Epidermolysis bullosa hereditaria letalis: report of a case and probable ultrastructural defects.

I Hashimoto, I Anton-Lamprecht, P Meyburg.   

Abstract

A case of epidermolysis bullosa hereditaria letalis (Herlitz) is described. In accordance with findings in other cases of Herlitz disease blister formation occurs in form of junctional separation. Electron microscopic study revealed scarcity and abnormal structure of hemidesmosomes, which may play an important role in the pathomorphogenesis of junctional blistering.

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Year:  1976        PMID： 1270327

Source DB:  PubMed          Journal:  Helv Paediatr Acta        ISSN： 0018-022X


  3 in total

1.  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

2.  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

3.  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
  3 in total

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