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Epidermolysis bullosa simplex 5C, with pyloric atresia

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Description

EBSPA is an autosomal recessive genodermatosis characterized by severe skin blistering at birth and congenital pyloric atresia. Death usually occurs in infancy. In reports of 2 consensus meetings for EB, Fine et al. (2000, 2008) considered EBSPA to be a 'basal' form of simplex EB because the electron microscopy shows that skin cleavage occurs in the lower basal level of the keratinocyte, just above the hemidesmosome. There is often decreased integration of keratin filaments with hemidesmosomes.

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

2,291

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Genes

External Links

  • OMIM

    612138

  • Orphanet

    158684

  • HPO
  • Medgen

    C2677349

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