Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
|
| pubmed:dateCreated |
1997-6-24
|
| pubmed:abstractText |
We report on an 11-year-old boy with distinct facial anomalies, iris coloboma, iris hypoplasia, cataract, high myopia, retinal detachment, moderate sensorineural hearing loss, and proteinuria. He appears to have the facio-oculo-acoustico-renal (FOAR) syndrome, a rare familial disorder reported only 4 times previously. In contrast to the other patients, he has normal intellect.
|
| pubmed:grant | |
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Mar
|
| pubmed:issn |
0148-7299
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
3
|
| pubmed:volume |
69
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
45-9; discussion 44
|
| pubmed:dateRevised |
2007-11-14
|
| pubmed:meshHeading |
pubmed-meshheading:9066882-Abnormalities, Multiple,
pubmed-meshheading:9066882-Adolescent,
pubmed-meshheading:9066882-Face,
pubmed-meshheading:9066882-Hearing Loss, Sensorineural,
pubmed-meshheading:9066882-Humans,
pubmed-meshheading:9066882-Male,
pubmed-meshheading:9066882-Proteinuria,
pubmed-meshheading:9066882-Retinal Detachment,
pubmed-meshheading:9066882-Syndrome
|
| pubmed:year |
1997
|
| pubmed:articleTitle |
Facio-oculo-acoustico-renal (FOAR) syndrome: case report and review.
|
| pubmed:affiliation |
Department of Medicine, University of Washington School of Medicine, Seattle, USA.
|
| pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Review,
Case Reports
|