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ISSN 2992-8559 (Electronic)
ISSN 1405-0625 (Print)

2014, Number 2

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Cir Plast 2014; 24 (2)

Surgical treatment of pseudosyndactyly in patients with recessive dystrophic epidermolysis bullosa

Gutiérrez SJE, Euán VCI

Language: Spanish
References: 7
Page: 113-114
PDF size: 184.30 Kb.


Text Extraction

No abstract


REFERENCES

  1. Fine JD, Eady RA, Bauer JW, Bruckner-Tuderman L, Heagerty A et al. The classification of inherited epidermolysis bullosa (EA): report of the Third International Consensus Meeting on Diagnosis and Classification of EA. J Am Acad Dermatol. 2008; 58: 931-950.

  2. Marincovich MP. Epidermolysis bullosa. eMedicine (serie en internet); 2007 [consultado 01-09-2008]. Disponible en: http://www.emedicine.com/derm/topic124.htm

  3. Fine JD, Johnson LB, Weiner M, Suchindran C. Cause-specific risk of childhood death in inherited epidermolysis bullosa. Pediatr. 2008; 152: 276-280.

  4. Das BB, Sahoo S. Dystrophic epidermolysis bullosa. J Perinatol. 2004; 24: 41-47.

  5. Pourreyron C, Cox G, Mao X, Volz A, Baksh N, Wong T et al. Patients with recessive dystrophic epidermolysis bullosa develop squamous-cell carcinoma regardless of type VII collagen expression. Invest Dermatol. 2007; 127: 2438-2444.

  6. Eisenberg M, Llewelyn D. Surgical management of hands in children with recessive dystrophic epidermolysis bullosa: use of allogenic composite cultured skin grafts. Br J Plast Surg. 1998; 51 (8): 608-613.

  7. Ferrari S, Pellegrini G, Mavilio F, De Luca M. Gene therapy approaches for epidermolysis bullosa. Clin Dermatol. 2005; 23: 430-436.




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