|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
10
|
|
pubmed:dateCreated |
2003-12-23
|
|
pubmed:abstractText |
GAPO syndrome is a rare autosomal recessive disorder whose main manifestations are: growth retardation, alopecia, pseudoanodontia and optic atrophy. We report here the ophthalmological findings in a 12-year-old Tunisian boy suffering from typical GAPO syndrome.
|
|
pubmed:language |
fre
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Dec
|
|
pubmed:issn |
0181-5512
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
26
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
1067-70
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:14691402-Abnormalities, Multiple,
pubmed-meshheading:14691402-Alopecia,
pubmed-meshheading:14691402-Anodontia,
pubmed-meshheading:14691402-Child,
pubmed-meshheading:14691402-Eye Diseases,
pubmed-meshheading:14691402-Growth Disorders,
pubmed-meshheading:14691402-Humans,
pubmed-meshheading:14691402-Male,
pubmed-meshheading:14691402-Optic Atrophy,
pubmed-meshheading:14691402-Syndrome,
pubmed-meshheading:14691402-Tunisia
|
|
pubmed:year |
2003
|
|
pubmed:articleTitle |
[Ocular manifestation in GAPO syndrome. Report of the first tunisian case].
|
|
pubmed:affiliation |
Service d'Ophtalmologie, Hôpital Universitaire de Charles Nicolle, Tunis, Tunisie. fr.touzri@gnet.tn
|
|
pubmed:publicationType |
Journal Article,
English Abstract,
Review,
Case Reports
|
