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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1979-5-23
|
| pubmed:abstractText |
The first case of trisomy of probable 12p mosaicism originated de novo is presented. Comparison of the clinical findings of this patient with those of previously described cases of 12p trisomy derived from translocated chromosomes indicates that the symptoms of 12p trisomy are: (1) normal birth weight and physical development, (2) severe psychomotor retardation and generalized hypotonia, (3) peculiarly round face with prominent cheeks, hypertelorism, epicanthus, broad, flat nasal bridge, short nose with anteverted nostrils, large philtrum, broad, prominent lower lip, and (4) poly(syn)dactyly of feet.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jan
|
| pubmed:issn |
0340-6717
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
25
|
| pubmed:volume |
46
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
135-40
|
| pubmed:dateRevised |
2011-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:422196-Chromosome Banding,
pubmed-meshheading:422196-Chromosomes, Human, 6-12 and X,
pubmed-meshheading:422196-Face,
pubmed-meshheading:422196-Foot Deformities, Congenital,
pubmed-meshheading:422196-Humans,
pubmed-meshheading:422196-Hypertelorism,
pubmed-meshheading:422196-Infant,
pubmed-meshheading:422196-Intellectual Disability,
pubmed-meshheading:422196-Male,
pubmed-meshheading:422196-Mosaicism,
pubmed-meshheading:422196-Syndrome,
pubmed-meshheading:422196-Trisomy
|
| pubmed:year |
1979
|
| pubmed:articleTitle |
Trisomy 12p syndrome: de novo occurrence of mosaic trisomy 12p in a mentally retarded boy.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|