Document Detail


Extreme microglossia.
MedLine Citation:
PMID:  12697349     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The congenital anomaly of extreme microglossia is uncommon and fewer than 50 cases have been described. The microglossia has often occurred in association with limb abnormalities and, therefore, these cases have been grouped together as the hypoglossia-hypodactylia syndrome within the oromandibular-limb hypogenesis syndromes. We present five cases seen at our referral centre. Surprisingly for this number none had limb anomalies but all had marked micrognathia-Gorlin-Hall classification type 5-two requiring tracheostomy for upper airway obstruction. All required tube feeding for between 4 and 17 months. Long term follow-up is not yet available.
Authors:
M A Thorp; P J de Waal; C A J Prescott
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  International journal of pediatric otorhinolaryngology     Volume:  67     ISSN:  0165-5876     ISO Abbreviation:  Int. J. Pediatr. Otorhinolaryngol.     Publication Date:  2003 May 
Date Detail:
Created Date:  2003-04-16     Completed Date:  2003-10-10     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  8003603     Medline TA:  Int J Pediatr Otorhinolaryngol     Country:  Ireland    
Other Details:
Languages:  eng     Pagination:  473-7     Citation Subset:  IM    
Affiliation:
Department of Otolaryngology, ENT Department, The Red Cross War Memorial Children's Hospital, University of Cape Town, Klipfontein Road, Rondebosch 7700, South Africa.
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MeSH Terms
Descriptor/Qualifier:
Airway Obstruction / etiology,  surgery
Enteral Nutrition
Female
Humans
Infant, Newborn
Male
Micrognathism / classification,  complications*,  therapy
Tongue / abnormalities*
Tracheostomy

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


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