pubmed-article:7058445 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:7058445 | lifeskim:mentions | umls-concept:C0000768 | lld:lifeskim |
pubmed-article:7058445 | lifeskim:mentions | umls-concept:C0431406 | lld:lifeskim |
pubmed-article:7058445 | lifeskim:mentions | umls-concept:C0224113 | lld:lifeskim |
pubmed-article:7058445 | lifeskim:mentions | umls-concept:C0243069 | lld:lifeskim |
pubmed-article:7058445 | lifeskim:mentions | umls-concept:C0332197 | lld:lifeskim |
pubmed-article:7058445 | lifeskim:mentions | umls-concept:C1561577 | lld:lifeskim |
pubmed-article:7058445 | lifeskim:mentions | umls-concept:C1514811 | lld:lifeskim |
pubmed-article:7058445 | lifeskim:mentions | umls-concept:C1706462 | lld:lifeskim |
pubmed-article:7058445 | pubmed:issue | 7 | lld:pubmed |
pubmed-article:7058445 | pubmed:dateCreated | 1982-4-12 | lld:pubmed |
pubmed-article:7058445 | pubmed:abstractText | An asymmetrical crying facies due to hypoplasia or absence of the depressor anguli oris muscle (DAOM) was observed in 23 infants and children. The cases were divided into two groups. Group 1 consisted of 12 patients who had associated cardiac abnormalities. In group 2 were 11 patients who either had other non-cardiac abnormalities (6) or no other abnormalities (5). The associated cardiac anomalies recorded in the literature are reviewed and 2 infants in this series are reported with abnormalities not previously described. The results of chromosomal analysis have generally been found to be normal, although a patient in our series was found to have trisomy E (18). The incidence of hypoplasia of the DAOM in newborn infants in a maternity hospital hospital is assessed and was found to be lower than reported in other studies. It is concluded that a detailed and careful examination for congenital abnormalities should be carried out on every child with an asymmetrical crying facies. | lld:pubmed |
pubmed-article:7058445 | pubmed:language | eng | lld:pubmed |
pubmed-article:7058445 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7058445 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:7058445 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:7058445 | pubmed:month | Feb | lld:pubmed |
pubmed-article:7058445 | pubmed:issn | 0256-9574 | lld:pubmed |
pubmed-article:7058445 | pubmed:author | pubmed-author:LevinS ESE | lld:pubmed |
pubmed-article:7058445 | pubmed:author | pubmed-author:MilnerSS | lld:pubmed |
pubmed-article:7058445 | pubmed:author | pubmed-author:SilvermanN... | lld:pubmed |
pubmed-article:7058445 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:7058445 | pubmed:day | 13 | lld:pubmed |
pubmed-article:7058445 | pubmed:volume | 61 | lld:pubmed |
pubmed-article:7058445 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:7058445 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:7058445 | pubmed:pagination | 227-31 | lld:pubmed |
pubmed-article:7058445 | pubmed:dateRevised | 2004-11-17 | lld:pubmed |
pubmed-article:7058445 | pubmed:meshHeading | pubmed-meshheading:7058445-... | lld:pubmed |
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pubmed-article:7058445 | pubmed:meshHeading | pubmed-meshheading:7058445-... | lld:pubmed |
pubmed-article:7058445 | pubmed:meshHeading | pubmed-meshheading:7058445-... | lld:pubmed |
pubmed-article:7058445 | pubmed:meshHeading | pubmed-meshheading:7058445-... | lld:pubmed |
pubmed-article:7058445 | pubmed:year | 1982 | lld:pubmed |
pubmed-article:7058445 | pubmed:articleTitle | Hypoplasia or absence of the depressor anguli oris muscle and congenital abnormalities, with special reference to the cardiofacial syndrome. | lld:pubmed |
pubmed-article:7058445 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:7058445 | pubmed:publicationType | Case Reports | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:7058445 | lld:pubmed |