| pubmed-article:15538081 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15538081 | lifeskim:mentions | umls-concept:C0241888 | lld:lifeskim |
| pubmed-article:15538081 | lifeskim:mentions | umls-concept:C0439660 | lld:lifeskim |
| pubmed-article:15538081 | lifeskim:mentions | umls-concept:C0684224 | lld:lifeskim |
| pubmed-article:15538081 | lifeskim:mentions | umls-concept:C0022579 | lld:lifeskim |
| pubmed-article:15538081 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:15538081 | pubmed:dateCreated | 2004-11-11 | lld:pubmed |
| pubmed-article:15538081 | pubmed:abstractText | Hereditary palmoplantar keratoderma, a well-known clinical entity, is illustrated through a familial report of an unmarried young man who is the product of a consanguineous marriage (paternal and maternal grandmothers were sisters). The lesions were characterized by immense yellow waxy thickening of the skin surrounded by erythematous border (halo) and fissures/cracks associated with extensive scaling of the palms and soles. The lesions were bilateral and symmetrical. These features were supported by orthokeratotic hyperkeratosis hypergranulosis and acanthosis in hematoxylin-eosin stained tissue sections prepared from the soles. Mycelia/spores could not be identified on Periodic acid-Schiff (PAS) reaction. An autosomal dominant trait was revealed through family pedigree. An abridged update to recap the current status is highlighted. | lld:pubmed |
| pubmed-article:15538081 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15538081 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15538081 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15538081 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15538081 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15538081 | pubmed:issn | 1540-9740 | lld:pubmed |
| pubmed-article:15538081 | pubmed:author | pubmed-author:SardanaKabirK | lld:pubmed |
| pubmed-article:15538081 | pubmed:author | pubmed-author:SehgalVirendr... | lld:pubmed |
| pubmed-article:15538081 | pubmed:author | pubmed-author:SharmaSonalS | lld:pubmed |
| pubmed-article:15538081 | pubmed:author | pubmed-author:RautDharmendr... | lld:pubmed |
| pubmed-article:15538081 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15538081 | pubmed:volume | 3 | lld:pubmed |
| pubmed-article:15538081 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15538081 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15538081 | pubmed:pagination | 323-30; quiz 331-2 | lld:pubmed |
| pubmed-article:15538081 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:15538081 | pubmed:meshHeading | pubmed-meshheading:15538081... | lld:pubmed |
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| pubmed-article:15538081 | pubmed:articleTitle | Hereditary palmoplantar (epidermolytic) keratoderma: illustration through a familial report. | lld:pubmed |
| pubmed-article:15538081 | pubmed:affiliation | Dermato-Venereology (Skin/VD) Centre, Sehgal Nursing Home, Panchwati, Azadpur, Delhi, India. drsehgal@ndf.vsnl.net.in. | lld:pubmed |
| pubmed-article:15538081 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15538081 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:15538081 | pubmed:publicationType | Review | lld:pubmed |
