Recessive Bullous Dermolysis of the Newborn in Preterm Siblings with a Missense Mutation in Type VII Collagen-Reference-Cited by-同舟云学术

Recessive Bullous Dermolysis of the Newborn in Preterm Siblings with a Missense Mutation in Type VII Collagen

Published:2015-01-30 Issue:2 Volume:32 Page:e42-e47
ISSN:0736-8046
Container-title:Pediatric Dermatology
language:en
Short-container-title:Pediatr Dermatol

Author:

Boccaletti Valeria¹,Zambruno Giovanna²,Castiglia Daniele²,Magnani Cinzia³,Tognetti Elena¹,Fabrizi Giuseppe¹,Cortelazzi Chiara¹,Pagliarello Calogero¹,Di Nuzzo Sergio¹

Affiliation:

1. Department of Dermatology; Parma University Hospital; Parma Italy

2. Laboratory of Molecular and Cell Biology; Istituto Dermopatico dell'Immacolata-IRCSS; Rome Italy

3. Neonatal Intensive Care Unit; Parma University Hospital; Parma Italy

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/pde.12513/fullpdf

Reference30 articles.

1. Transient bullous dermolysis of the newborn;Hashimoto;Arch Dermatol,1985

2. The classification of inherited epidermolysis bullosa (EB): report of the Third International Consensus Meeting on Diagnosis and Classification of EB;Fine;J Am Acad Dermatol,2008

3. Genetic basis of dominantly inherited transient bullous dermolysis of the newborn: a splice site mutation in the type VII collagen gene;Christiano;J Invest Dermatol,1997

4. Denaturing HPLC-based approach for detection of COL7A1 gene mutations causing dystrophic epidermolysis bullosa;Posteraro;Biochem Biophys Res Commun,2005

5. Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification;Fine;J Am Acad Dermatol,2014

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