Document Detail


Michel's anomaly, type I microtia and microdontia.
MedLine Citation:
PMID:  2044484     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
J H Hersh; T M Ganzel; R A Fellows
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Ear, nose, & throat journal     Volume:  70     ISSN:  0145-5613     ISO Abbreviation:  Ear Nose Throat J     Publication Date:  1991 Mar 
Date Detail:
Created Date:  1991-07-17     Completed Date:  1991-07-17     Revised Date:  2005-11-17    
Medline Journal Info:
Nlm Unique ID:  7701817     Medline TA:  Ear Nose Throat J     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  155-7     Citation Subset:  IM    
Affiliation:
Department of Pediatrics, Child Evaluation Center, Louisville, Kentucky.
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MeSH Terms
Descriptor/Qualifier:
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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