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Globalization of DNA-based prenatal diagnosis for recessive dystrophic epidermolysis bullosa

โœ Scribed by V. Wessagowit; A. Chunharas; D. Wattanasirichaigoon; J. A. McGrath


Book ID
108694445
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
158 KB
Volume
32
Category
Article
ISSN
0307-6938

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Epidermolysis bullosa (EB) is a group of heritable diseases which manifest with blistering and erosions of the skin and mucous membranes. Due to life-threatening complications and significant long-term morbidity associated with the severe, neonatal lethal (Herlitz) form of junctional EB (H-JEB), the

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Epidermolysis bullosa simplex (EBS) is a skin fragility disorder in which mild physical trauma leads to blistering. The phenotype of the disorder is variable, from relatively mild affecting only the hands and/or feet, to very severe with widespread blistering. For the severest forms of EBS there is