Document Detail

Methaemoglobinaemia with G6PD deficiency: rare cause of persistently low saturations in neonates.
MedLine Citation:
PMID:  21418105     Owner:  NLM     Status:  MEDLINE    
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.
Hannah Titheradge; Katie Nolan; Shanmugasundaram Sivakumar; Srinivas Bandi
Related Documents :
7576395 - White coat hypertension and white coat effect. similarities and differences.
8924265 - Urinary n-acetyl-beta-d-glucosaminidase changes in relation to age, sex, race, and dias...
2560975 - Race, borderline hypertension, and hemodynamic responses to behavioral stress before an...
18844765 - Anger types: heritability and relation to blood pressure, body mass index, and left ven...
12695415 - Pressure wave reflection assessed from the peripheral pulse: is a transfer function nec...
1437355 - Intratracheal administration of pulmonary vasodilator agents.
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.
Department of Paediatrics, Sandwell & West Birmingham NHS Hospitals Trust, Birmingham, UK.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Diagnosis, Differential
Exchange Transfusion, Whole Blood
Glucosephosphate Dehydrogenase Deficiency / complications*
Hyperbilirubinemia / therapy
Infant, Newborn
Infant, Premature
Methemoglobinemia / complications*
Oxygen / administration & dosage,  blood*
Respiration, Artificial
Respiratory Distress Syndrome, Newborn / etiology*
Reg. No./Substance:

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

Previous Document:  Role of angiotensin-converting enzyme gene polymorphism in persistent pulmonary hypertension of the ...
Next Document:  The impact of CYP3A5*3 on risk and prognosis in childhood acute lymphoblastic leukemia.