Article
Long-term follow-up of patients with recessive dystrophic epidermolysis bullosa in the Netherlands: expansion of the mutation database and unusual phenotype-genotype correlations.
Journal of dermatological science - 1 Oct 2009
van den Akker Peter C, van Essen Anthonie J, Kraak Marian M J, Meijer Rowdy, Nijenhuis Miranda, Meijer Gonnie, Hofstra Robert M W, Pas Hendri H, Scheffer Hans, Jonkman Marcel F
Abstract excerpt
BACKGROUND: The current classification of recessive dystrophic epidermolysis bullosa (RDEB) comprises two major subtypes: 'severe generalized RDEB' (RDEB-sev gen) with early-onset, extensive, generalized blistering and scarring, complete absence of type VII collagen, and bi-allelic COL7A1 null mutations; milder 'generalized other RDEB' (RDEB-O) with reduced-to-normal type VII collagen expression, and non-null...
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