Globalization of DNA-based prenatal diagnosis for recessive dystrophic epidermolysis bullosa
โ 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
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
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
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