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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
1991-2-22
|
| pubmed:abstractText |
We report two cases of C.M.T.C., a rare cutaneous vascular anomaly, which is manifested at birth. It is a rare birth defect of unknown etiology; usually occurs sporadically. There is an association of C.M.T.C. with other congenital anomalies in at least 50% of the patients. On the basis of two cases, the clinical features of cutis marmorata telangiectasica congenita are described and the differential diagnosis discussed.
|
| pubmed:language |
ita
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0391-5387
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
12
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
285-7
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading | |
| pubmed:articleTitle |
[Cutis marmorata telangiectasica congenita. Description of 2 further cases].
|
| pubmed:affiliation |
Nuovo Ospedale San Giovanni di Dio, U.S.L. 10/C, Firenze, Italia.
|
| pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|