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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1991-1-10
|
| pubmed:abstractText |
We report on a boy with a characteristic combination of facial anomalies, syndactylies of fingers and toes, and mental retardation. Scott et al. (Journal of Pediatrics 78:658-663, 1971) observed 3 brothers with almost identical manifestations. The mother of these patients had bilateral syndactyly of toes 2 and 3. This led the authors to suggest X-linked inheritance. The mother of our patient also has cutaneous syndactyly between the second and third toes, strengthening the hypothesis of X-linked inheritance.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Oct
|
| pubmed:issn |
0148-7299
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
37
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
224-6
|
| pubmed:dateRevised |
2011-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:2174209-Face,
pubmed-meshheading:2174209-Fingers,
pubmed-meshheading:2174209-Follow-Up Studies,
pubmed-meshheading:2174209-Genetic Linkage,
pubmed-meshheading:2174209-Humans,
pubmed-meshheading:2174209-Infant, Newborn,
pubmed-meshheading:2174209-Intellectual Disability,
pubmed-meshheading:2174209-Male,
pubmed-meshheading:2174209-Skull,
pubmed-meshheading:2174209-Syndactyly,
pubmed-meshheading:2174209-Syndrome,
pubmed-meshheading:2174209-Toes,
pubmed-meshheading:2174209-X Chromosome
|
| pubmed:year |
1990
|
| pubmed:articleTitle |
The craniodigital syndrome of Scott: report of a second family.
|
| pubmed:affiliation |
Department of Clinical Genetics, Medical Academy Dresden Carl Gustav Carus, German Democratic Republic.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|