3284470

Source:http://linkedlifedata.com/resource/pubmed/id/3284470

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0009566, umls-concept:C0014527, umls-concept:C0332307
pubmed:issue	5
pubmed:dateCreated	1988-6-9
pubmed:abstractText	The various epidermolysis bullosa syndromes are classified into (1) epidermolytic, (2) lamina lucidolytic (junctional), and (3) dermolytic (dystrophic) subgroups. The mode of inheritance and the clinical manifestations, both cutaneous and noncutaneous, are systematically summarized. This report provides an overview of the diverse epidermolysis bullosa syndromes, particularly from the perspective of their nondermatological manifestations.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0372433
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0003-987X
pubmed:author	pubmed-author:PearsonR WRW
pubmed:issnType	Print
pubmed:volume	124
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	718-25
pubmed:dateRevised	2008-3-17
pubmed:meshHeading	pubmed-meshheading:3284470-Child, pubmed-meshheading:3284470-Child, Preschool, pubmed-meshheading:3284470-Epidermolysis Bullosa, pubmed-meshheading:3284470-Humans, pubmed-meshheading:3284470-Infant, pubmed-meshheading:3284470-Infant, Newborn, pubmed-meshheading:3284470-Skin
pubmed:year	1988
pubmed:articleTitle	Clinicopathologic types of epidermolysis bullosa and their nondermatological complications.
pubmed:affiliation	Department of Dermatology, Rush-Presbyterian-St Luke's Medical Center, Chicago, IL 60612.
pubmed:publicationType	Journal Article, Review