Document Detail


Methaemoglobinaemia with G6PD deficiency: rare cause of persistently low saturations in neonates.
MedLine Citation:
PMID:  21418105     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
CONCLUSION: Paediatricians should remember that methaemoglobinaemia is a rare but important cause of persistently low saturations, and exchange transfusion is a reliable treatment for this condition.
Authors:
Hannah Titheradge; Katie Nolan; Shanmugasundaram Sivakumar; Srinivas Bandi
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Acta paediatrica (Oslo, Norway : 1992)     Volume:  100     ISSN:  1651-2227     ISO Abbreviation:  Acta Paediatr.     Publication Date:  2011 Jul 
Date Detail:
Created Date:  2011-06-03     Completed Date:  2011-09-08     Revised Date:  2013-05-20    
Medline Journal Info:
Nlm Unique ID:  9205968     Medline TA:  Acta Paediatr     Country:  Norway    
Other Details:
Languages:  eng     Pagination:  e47-8     Citation Subset:  IM    
Copyright Information:
© 2011 The Author(s)/Acta Paediatrica © 2011 Foundation Acta Paediatrica.
Affiliation:
Department of Paediatrics, Sandwell & West Birmingham NHS Hospitals Trust, Birmingham, UK.
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MeSH Terms
Descriptor/Qualifier:
Diagnosis, Differential
Exchange Transfusion, Whole Blood
Glucosephosphate Dehydrogenase Deficiency / complications*
Humans
Hyperbilirubinemia / therapy
Infant, Newborn
Infant, Premature
Male
Methemoglobinemia / complications*
Oxygen / administration & dosage,  blood*
Phototherapy
Respiration, Artificial
Respiratory Distress Syndrome, Newborn / etiology*
Chemical
Reg. No./Substance:
7782-44-7/Oxygen

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


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