Neonatal Junctional Epidermolysis Bullosa: Treatment Conundrums and Ethical Decision Making

Author:

Yang Catherine S.,Kroshinksy Daniela,Cummings Brian M.

Publisher

Springer Science and Business Media LLC

Subject

Dermatology,General Medicine

Reference43 articles.

1. Fine JD, Bruckner-Tuderman L, Eady RAJ, et al. Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification. J Am Acad Dermatol. 2014;70:1103–26.

2. Fine JD, Johnson LB, Suchindran C, et al. The epidemiology of inherited epidermolysis bullosa. Findings in U.S., Canadian, and European study populations. In: Fine JD, Bauer EA, McGuire J, Moshell A, editors. Epidermolysis bullosa: clinical, epidemiologic, and laboratory advances and the findings of the National Epidermolysis Bullosa Registry. Baltimore: Johns Hopkins University Press; 1999. p. 101–13.

3. Castori M, Floriddia G, De Luca N, et al. Herlitz junctional epidermolysis bullosa: laminin-5 mutational profile and carrier frequency in the Italian population. Br J Dermatol. 2008;158:38–44.

4. Yuen WY, Lemmink HH, van Dijk-Bos KK, et al. Herlitz junctional epidermolysis bullosa: diagnostic features, mutational profile, incidence and population carrier frequency in the Netherlands. Br J Dermatol. 2011;165:1314–22.

5. Kelly-Mancuso G, Kopelan B, Azizkhan RG, et al. Junctional epidermolysis bullosa incidence and survival: 5-year experience of the Dystrophic Epidermolysis Bullosa Research Association of America (DebRA) nurse educator, 2007 to 2011. Pediatr Dermatol. 2014;31:159–62.

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