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PRENATAL DIAGNOSIS OF JUNCTIONAL EPIDERMOLYSIS BULLOSA HERLITZ TYPE

✍ Scribed by Hausser, I.; Anton-Lamprecht, I.; Gustavii, B.

Book ID: 122809947
Publisher: The Lancet
Year: 1989
Tongue: English
Weight: 523 KB
Volume: 334
Category: Article
ISSN: 0140-6736
DOI: 10.1016/S0140-6736(89)91037-4

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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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