Document Detail


Congenital arhinia: case report of a rare congenital anomaly.
MedLine Citation:
PMID:  21888462     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Congenital absence of the nose or arhinia is a rare defect of embryogenesis often associated with other anomalies. Arhinia is a life-threatening condition that requires a highly skilled neonatal resuscitation team in the delivery room. The associated anomalies often have a significant effect on the immediate as well as long-term outcome of the neonate. This report presents a case of congenital arhinia and reviews the management of such cases.
Authors:
Seyed Hossein Fakhraee; Shahin Nariman; Reza Taghipour
Publication Detail:
Type:  Case Reports; Journal Article; Review    
Journal Detail:
Title:  Archives of Iranian medicine     Volume:  14     ISSN:  1735-3947     ISO Abbreviation:  Arch Iran Med     Publication Date:  2011 Sep 
Date Detail:
Created Date:  2011-09-05     Completed Date:  2011-11-21     Revised Date:  2013-05-15    
Medline Journal Info:
Nlm Unique ID:  100889644     Medline TA:  Arch Iran Med     Country:  Iran    
Other Details:
Languages:  eng     Pagination:  355-6     Citation Subset:  IM    
Affiliation:
Department of Neonatology, Mofid Children's Hospital, Tehran, Iran.
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MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple* / embryology,  therapy
Congenital Abnormalities* / physiopathology,  radiography,  therapy
Disease Management
Eye Abnormalities / radiography*
Fatal Outcome
Humans
Infant, Newborn
Intensive Care Units, Neonatal
Magnetic Resonance Imaging
Male
Nose / abnormalities*,  physiopathology,  radiography
Rare Diseases
Respiration, Artificial / adverse effects*
Sepsis / etiology*
Tomography, X-Ray Computed
Tracheostomy
Ultrasonography, Prenatal

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


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