Literature DB >> 8954268

The genetic basis of hereditary blistering disorders.

A S Paller1.   

Abstract

Inherited blistering disorders have been classified by inheritance pattern, ultrastructural morphology and level of skin cleavage, and immunofluorescence detection of cutaneous antigens. During the past 5 years, investigators have discovered the molecular bases for the major inherited blistering disorders, epidermolytic hyperkeratosis, epidermolysis bullosa simplex, epidermolytic palmoplantar keratoderma, junctional epidermolysis bullosa, and dystrophic forms of epidermolysis bullosa. In addition to providing answers to patients about the underlying mechanisms of these devastating blistering disorders, the discoveries have provided insight into the function of several cutaneous proteins and have led to the ability to diagnose prenatally these lifelong conditions through genetic analysis in affected families.

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Year:  1996        PMID: 8954268     DOI: 10.1097/00008480-199608000-00011

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  3 in total

Review 1.  Gene therapy for skin diseases.

Authors:  Emily Gorell; Ngon Nguyen; Alfred Lane; Zurab Siprashvili
Journal:  Cold Spring Harb Perspect Med       Date:  2014-04-01       Impact factor: 6.915

2.  Long-term type VII collagen restoration to human epidermolysis bullosa skin tissue.

Authors:  Zurab Siprashvili; Ngon T Nguyen; Maria Y Bezchinsky; M Peter Marinkovich; Alfred T Lane; Paul A Khavari
Journal:  Hum Gene Ther       Date:  2010-10       Impact factor: 5.695

3.  Dystrophic epidermolysis bullosa in a child.

Authors:  Uma Eswara
Journal:  Contemp Clin Dent       Date:  2012-01
  3 in total

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