Source:http://linkedlifedata.com/resource/pubmed/id/11694224
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
2001-11-5
|
| pubmed:abstractText |
We describe two patients (first cousins, once removed) with an unusual head shape, high arched palate, flat nasal bridge, abnormal ears, hand and feet abnormalities and other anomalies. The patients were ascertained independently and it was initially unknown that they were related to each other. Cytogenetic and fluorescent in situ hybridization (FISH) analysis identified a der(2)t(2;10)(q37.3;q24.1) unbalanced translocation resulting in loss of 2q37.3-qter and duplication 10q24.1-qter. The clinical features of these two patients are compared with previously described cases of 2q deletion and 10q duplication. These patients also emphasize the difficulty in some families of understanding and sharing genetic information and in the difficulties in obtaining an accurate pedigree in a genetics clinic.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0003-3995
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
44
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
129-34
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| pubmed:dateRevised |
2004-11-17
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| pubmed:meshHeading |
pubmed-meshheading:11694224-Adolescent,
pubmed-meshheading:11694224-Chromosome Banding,
pubmed-meshheading:11694224-Chromosome Deletion,
pubmed-meshheading:11694224-Chromosomes, Human, Pair 10,
pubmed-meshheading:11694224-Chromosomes, Human, Pair 2,
pubmed-meshheading:11694224-Face,
pubmed-meshheading:11694224-Facies,
pubmed-meshheading:11694224-Family Health,
pubmed-meshheading:11694224-Female,
pubmed-meshheading:11694224-Foot Deformities, Congenital,
pubmed-meshheading:11694224-Gene Duplication,
pubmed-meshheading:11694224-Hand Deformities, Congenital,
pubmed-meshheading:11694224-Humans,
pubmed-meshheading:11694224-In Situ Hybridization, Fluorescence,
pubmed-meshheading:11694224-Infant,
pubmed-meshheading:11694224-Karyotyping,
pubmed-meshheading:11694224-Male,
pubmed-meshheading:11694224-Pedigree,
pubmed-meshheading:11694224-Syndrome,
pubmed-meshheading:11694224-Translocation, Genetic
|
| pubmed:articleTitle |
Deletion of 2q37 and duplication of 10q24: two cases in the same family and review of the literature.
|
| pubmed:affiliation |
Department of Medical Genetics, Henry Ford Health System, 2799 W. Grand Blvd. CFP4, Detroit, Michigan 48202, USA.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|