Source:http://linkedlifedata.com/resource/pubmed/id/20496833
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5-6
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pubmed:dateCreated |
2010-5-25
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pubmed:abstractText |
A male black and white German Holstein calf showed a congenital, high-graded scoliosis and rotation of the thoracal spinal cord associated with shortening and fusion of multiple vertebral bodies and abnormal bending of the processus spinosus. Furthermore reduced birth weight, partial hypoplasia of the lung, excessive liver segmentation, doubled gall bladder, rectal atresia, horseshoe kidney, and uterine atresia were found. Due to the exclusion of a point mutation in exon 4 of the solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member A3 (SLC35A3) gene, complex vertebral malformation (CVM) was ruled out. Conclusively, it is hypothetized that the presented case resembles a new brachyspina syndrome with a still unresolved genetic etiology.
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pubmed:language |
ger
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0005-9366
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
123
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
251-5
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pubmed:meshHeading |
pubmed-meshheading:20496833-Animals,
pubmed-meshheading:20496833-Cattle,
pubmed-meshheading:20496833-Exons,
pubmed-meshheading:20496833-Fatal Outcome,
pubmed-meshheading:20496833-Male,
pubmed-meshheading:20496833-Monosaccharide Transport Proteins,
pubmed-meshheading:20496833-Point Mutation,
pubmed-meshheading:20496833-Scoliosis,
pubmed-meshheading:20496833-Spine,
pubmed-meshheading:20496833-Uridine Diphosphate N-Acetylglucosamine
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pubmed:articleTitle |
[Vertebral and multiple organ malformations in a black and white German Holstein calf].
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pubmed:affiliation |
Institut fürTierzucht und Vererbungsforschung, Stiftung Tierärztliche Hochschule Hannover.
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
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