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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1980-6-25
|
| pubmed:abstractText |
A new case of the Baller-Gerold syndrome is described in a 6 1/2-year-old, black male who presented at birth with bilateral synostoses of the coronal and lambdoidal sutures, bilateral radial aplasia, vertebral anomalies and genito-urinary malformations. The parents and siblings were unaffected, and there was no history of consanguinity. A review of the history and physical findings in our patient and in the four other patients previously reported in the literature is provided, with a discussion on pathogenesis, prognosis and the possible autosomal recessive mode of inheritance of the syndrome.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Feb
|
| pubmed:issn |
0009-9163
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
17
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
161-6
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:7363501-Abnormalities, Multiple,
pubmed-meshheading:7363501-Adolescent,
pubmed-meshheading:7363501-Adult,
pubmed-meshheading:7363501-Child,
pubmed-meshheading:7363501-Craniosynostoses,
pubmed-meshheading:7363501-Female,
pubmed-meshheading:7363501-Humans,
pubmed-meshheading:7363501-Infant, Newborn,
pubmed-meshheading:7363501-Male,
pubmed-meshheading:7363501-Radius,
pubmed-meshheading:7363501-Skull,
pubmed-meshheading:7363501-Syndrome
|
| pubmed:year |
1980
|
| pubmed:articleTitle |
Baller-Gerold syndrome craniosynostosis-radial aplasia syndrome.
|
| pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Case Reports
|