Literature DB >> 7615888

Fatal systemic amyloidosis (AA type) in two sisters with dystrophic epidermolysis bullosa.

J F Bourke1, G Browne, E F Gaffney, M Young.   

Abstract

Systemic amyloidosis is a rare but recognized complication of dystrophic epidermolysis bullosa. We report the cases of two siblings with recessive dystrophic epidermolysis bullosa who died of complications associated with systemic amyloidosis (AA type). This is the first report of systemic amyloidosis in siblings with dystrophic epidermolysis bullosa.

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Year:  1995        PMID： 7615888     DOI： 10.1016/0190-9622(95)91436-6

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN： 0190-9622            Impact factor:   11.527


  2 in total

1.  Recessive dystrophic epidermolysis bullosa (RDEB) complicated by secondary hepatic amyloidosis.

Authors:  Cassandra Chaptini; Genevieve Casey; Adam G Harris; Dedee F Murrell; Lynne Gordon
Journal:  JAAD Case Rep       Date:  2015-09-24

2.  Diffuse membranoproliferative glomerulonephritis with focal sclerosis and renal amyloidosis in an adult male with autosomal dominant dystrophic epidermolysis bullosa: a case report.

Authors:  Karim M Soliman; Tibor Fülöp; David W Ploth; Johann Herberth
Journal:  Ren Fail       Date:  2019-11       Impact factor: 2.606
  2 in total

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