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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1997-7-31
|
| pubmed:abstractText |
Epidermal nevus syndrome is characterized by congenital anomalies affecting multiple body systems, especially the skin, skeleton and central nervous system. A form of rickets/osteomalacia that is markedly resistant to treatment with vitamin D has been reported in children with this syndrome. We report the clinical and laboratory observations in a child with epidermal nevi and severe hypophosphatemic rickets/osteomalacia.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0041-4301
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
39
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
247-51
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:9223923-Adolescent,
pubmed-meshheading:9223923-Child,
pubmed-meshheading:9223923-Hamartoma,
pubmed-meshheading:9223923-Humans,
pubmed-meshheading:9223923-Hypophosphatemia,
pubmed-meshheading:9223923-Leg Length Inequality,
pubmed-meshheading:9223923-Male,
pubmed-meshheading:9223923-Osteomalacia,
pubmed-meshheading:9223923-Rickets,
pubmed-meshheading:9223923-Skin Diseases,
pubmed-meshheading:9223923-Syndrome
|
| pubmed:articleTitle |
Hypophosphatemic vitamin-D resistant rickets associated with epidermal nevus syndrome. A case report.
|
| pubmed:affiliation |
Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara.
|
| pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|