Document Detail


Hypoglossia congenita.
MedLine Citation:
PMID:  2311539     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Hypoglossia and aglossia are rare congenital malformations, especially when found as isolated abnormalities. In view of their usual association with other anomalies of the face, oral cavity, and distal extremities, an accurate investigation is required. We describe a 2-year-old girl with isolated hypoglossia and severe dental disease. Clinical understanding of the changes in the mechanisms of oral suction, mastication, swallowing, and speech, as well as the existing dental occlusion, requires a multidisciplinary team approach so that a more effective treatment can be administered.
Authors:
L L Weckx; D A Justino; Z C Guedes; L Y Weckx
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Ear, nose, & throat journal     Volume:  69     ISSN:  0145-5613     ISO Abbreviation:  Ear Nose Throat J     Publication Date:  1990 Feb 
Date Detail:
Created Date:  1990-04-17     Completed Date:  1990-04-17     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  7701817     Medline TA:  Ear Nose Throat J     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  108, 111-3     Citation Subset:  IM    
Affiliation:
Department of Ophthalmology-Otolaryngology, Escola Paulista de Medicina, São Paulo, Brazil.
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MeSH Terms
Descriptor/Qualifier:
Child, Preschool
Deglutition Disorders
Female
Humans
Malocclusion / complications*
Mastication
Tongue / abnormalities*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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