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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
1991-7-17
|
pubmed:abstractText |
Michel's anomaly is an extremely rare cause of congenital sensorineural hearing loss. We present a 2-1/2 year old white female with this inner ear defect associated with type I microtia and microdontia. Assessment of anatomic structures of the ear is critical in an infant with abnormal auditory brainstem responses to determine whether a structural lesion is present and the most appropriate rehabilitative approach available.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0145-5613
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
70
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
155-7
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pubmed:dateRevised |
2005-11-17
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pubmed:meshHeading |
pubmed-meshheading:2044484-Abnormalities, Multiple,
pubmed-meshheading:2044484-Ear, External,
pubmed-meshheading:2044484-Ear, Inner,
pubmed-meshheading:2044484-Female,
pubmed-meshheading:2044484-Humans,
pubmed-meshheading:2044484-Infant, Newborn,
pubmed-meshheading:2044484-Micrognathism,
pubmed-meshheading:2044484-Tooth Abnormalities
|
pubmed:year |
1991
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pubmed:articleTitle |
Michel's anomaly, type I microtia and microdontia.
|
pubmed:affiliation |
Department of Pediatrics, Child Evaluation Center, Louisville, Kentucky.
|
pubmed:publicationType |
Journal Article,
Case Reports
|