Document Detail


Agnathia (severe micrognathia), aglossia and choanal atresia in an infant.
MedLine Citation:
PMID:  7576899     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A neonate is reported here, who was born with severe mandibular hypoplasia, complete absence of the tongue, unilateral choanal atresia, contralateral choanal stenosis and developed severe airway obstruction at birth. Arrested development of the ventral first branchial arch most likely underlies the clinical deficits. Most reported cases of agnathia have been lethal but the infant reported here has survived into infancy with a tracheostomy and feeding gastrostomy. Her clinical features, assessment and management are discussed.
Authors:
P J Walker; M J Edwards; V Petroff; I Wilson; A D Temperley; J Seabrook
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Journal of paediatrics and child health     Volume:  31     ISSN:  1034-4810     ISO Abbreviation:  J Paediatr Child Health     Publication Date:  1995 Aug 
Date Detail:
Created Date:  1995-12-12     Completed Date:  1995-12-12     Revised Date:  2007-09-24    
Medline Journal Info:
Nlm Unique ID:  9005421     Medline TA:  J Paediatr Child Health     Country:  AUSTRALIA    
Other Details:
Languages:  eng     Pagination:  358-61     Citation Subset:  IM    
Affiliation:
Department of Paediatrics, John Hunter Hospital, Newcastle, New South Wales, Australia.
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MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple* / embryology,  pathology,  surgery
Choanal Atresia* / embryology,  pathology
Female
Humans
Infant, Newborn
Micrognathism* / embryology,  pathology
Tongue / abnormalities*,  embryology
Tracheostomy

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


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