Epidermolysis Bullosa Clinical, Epidemiologic, and Laboratory Advances, and the Findings of the National Epidermolysis Bullosa Registry

By:

National Epidermolysis Bullosa Registry (U.S.)

Contributor(s):

Jo-David Fine

Material type: Text

TextPublication details: London Johns Hopkins University Press, 1999 Original from the University of Michigan Digitized 19 Aug 2008 Edition: illustratedDescription: 490 pagesISBN:

0801860245
9780801860249

Subject(s):

DDC classification:

616.5 FIN

Summary: Inherited epidermolysis bullosa (EB) is a group of rare genetic diseases in which the skin is mechanically very fragile, resulting in chronic blister formation. In the most severe cases, affected persons may also experience disease involvement of other organs, cancer, and even premature death. This examination of EB employs a large research study population and uses epidemiological and biostatistical research principles. It also assesses more than 2000 patients with EB.

Item type: BOOKS

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Holdings
Item type	Current library	Collection	Call number	Status	Barcode
BOOKS	MWALIMU NYERERE LEARNING RESOURCES CENTRE-CUHAS BUGANDO	NFIC	616.5 FIN (Browse shelf(Opens below))	1	A. 8397

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Inherited epidermolysis bullosa (EB) is a group of rare genetic diseases in which the skin is mechanically very fragile, resulting in chronic blister formation. In the most severe cases, affected persons may also experience disease involvement of other organs, cancer, and even premature death. This examination of EB employs a large research study population and uses epidemiological and biostatistical research principles. It also assesses more than 2000 patients with EB.

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