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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
6
|
| pubmed:dateCreated |
1995-6-1
|
| pubmed:abstractText |
Complete nasal aplasia is an extremely rare clinical entity and most infants are stillborn when this is associated with holoprosencephaly. A viable 3-year-old infant born with frontonasal arrest without holoprosencephaly is presented. The child's main complaint was lack of a nasal airway, which made eating extremely difficult. A method for craniofacial reconstruction of the nasopharynx is presented.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
AIM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
May
|
| pubmed:issn |
0032-1052
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
95
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
1101-4
|
| pubmed:dateRevised |
2011-2-16
|
| pubmed:meshHeading |
pubmed-meshheading:7732122-Abnormalities, Multiple,
pubmed-meshheading:7732122-Child, Preschool,
pubmed-meshheading:7732122-Humans,
pubmed-meshheading:7732122-Male,
pubmed-meshheading:7732122-Microphthalmos,
pubmed-meshheading:7732122-Nasopharynx,
pubmed-meshheading:7732122-Nose,
pubmed-meshheading:7732122-Thumb
|
| pubmed:year |
1995
|
| pubmed:articleTitle |
Complete nasal agenesis with bilateral microphthalmia and unilateral duplication of the thumb.
|
| pubmed:affiliation |
Division of Plastic and Reconstructive Surgery, New York Hospital-Cornell Medical Center, New York, N.Y., USA.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|