Literature DB >> 5173253

Phenotype-genotype correlations in epidermolysis bullosa.

T Gedde-Dahl.   

Abstract

In Norway, epidermolysis bullosa (EB) has been studied from the clinical, genetic and epidemiologic viewpoints. Heterogeneity is found both in the EB simplex (EBS) and the EB dystrophica (EBD) group. One new EBS and two new EBD varieties were found in addition to previously known types. At least five nonidentical recessive EBD genes could be defined and suggestive evidence for allelism between some of them were found. A classification of hereditary EB is presented.

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Mesh：

Year:  1971        PMID： 5173253

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


  4 in total

1.  Pathology of collagen degradation. A review.

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

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 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

4.  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
  4 in total

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