15482301

Source:http://linkedlifedata.com/resource/pubmed/id/15482301

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0031911, umls-concept:C0406811
pubmed:issue	6
pubmed:dateCreated	2004-10-14
pubmed:abstractText	Dowling-Degos disease is a rare autosomal dominant inherited pigmentary disorder characterized by reticulate pigmentation of the flexures, prominent comedone like lesions and pitted scars. Dyschromatosis universalis hereditaria is characterized by the presence of hypopigmented as well as hyperpigmented macules. We report a family showing features of both these diseases.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9216037
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0926-9959
pubmed:author	pubmed-author:KanwarA JAJ, pubmed-author:SandhuKK, pubmed-author:SaraswatAA
pubmed:issnType	Print
pubmed:volume	18
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	702-4
pubmed:meshHeading	pubmed-meshheading:15482301-Adult, pubmed-meshheading:15482301-Female, pubmed-meshheading:15482301-Humans, pubmed-meshheading:15482301-Middle Aged, pubmed-meshheading:15482301-Pigmentation Disorders, pubmed-meshheading:15482301-Skin Diseases, Genetic
pubmed:year	2004
pubmed:articleTitle	Dowling-Degos disease with dyschromatosis universalis hereditaria-like pigmentation in a family.
pubmed:affiliation	Department of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Sector 12, Chandigarh, 160012, India. kd_sandhu@yahoo.co.in
pubmed:publicationType	Journal Article, Case Reports