| Michel's anomaly, type I microtia and microdontia. | |
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MedLine Citation:
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PMID: 2044484 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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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. |
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Authors:
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J H Hersh; T M Ganzel; R A Fellows |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Ear, nose, & throat journal Volume: 70 ISSN: 0145-5613 ISO Abbreviation: Ear Nose Throat J Publication Date: 1991 Mar |
Date Detail:
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Created Date: 1991-07-17 Completed Date: 1991-07-17 Revised Date: 2005-11-17 |
Medline Journal Info:
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Nlm Unique ID: 7701817 Medline TA: Ear Nose Throat J Country: UNITED STATES |
Other Details:
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Languages: eng Pagination: 155-7 Citation Subset: IM |
Affiliation:
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Department of Pediatrics, Child Evaluation Center, Louisville, Kentucky. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Abnormalities, Multiple* Ear, External / abnormalities* Ear, Inner / abnormalities* Female Humans Infant, Newborn Micrognathism Tooth Abnormalities* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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