Literature DB >> 488499

[Clinical aspects of epidermolyses with junctional blister formation (author's transl)].

U W Schnyder, I Anton-Lamprecht.   

Abstract

The clinical symptomatology of epidermolysis bullosa atrophicans generalisata gravis (Herlitz' disease), epidermolysis bullosa atrophicans generalisata mitis (typus Disentis) and epidermolysis bullosa atrophicans localisata is described. These types belong to the non-scarring epidermolyses and show ultrastructurally junctional blistering.

Entities:  

Mesh：

Year:  1979        PMID： 488499

Source DB:  PubMed          Journal:  Dermatologica        ISSN： 0011-9075


  2 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.  Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition.

Authors:  J A McGrath; B Gatalica; K Li; M G Dunnill; J R McMillan; A M Christiano; R A Eady; J Uitto
Journal:  Am J Pathol       Date:  1996-06       Impact factor: 4.307
  2 in total

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