Document Detail


Sickle-cell disease not identified by newborn screening because of prior transfusion.
MedLine Citation:
PMID:  10657834     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Erythrocyte transfusion can impair detection of sickle-cell disease, galactosemia, or biotinidase deficiency with newborn screening. We report on 4 infants with SCD in whom delayed diagnosis was associated with neonatal transfusion. In 2 cases, the initial newborn screening showed no hemoglobin S. In no case was the recommended screening >/=120 days from the last transfusion obtained. Two children had significant SCD-related morbidity before diagnosis.
Authors:
W Reed; P A Lane; F Lorey; J Bojanowski; M Glass; R R Louie; B H Lubin; E P Vichinsky
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Publication Detail:
Type:  Case Reports; Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  The Journal of pediatrics     Volume:  136     ISSN:  0022-3476     ISO Abbreviation:  J. Pediatr.     Publication Date:  2000 Feb 
Date Detail:
Created Date:  2000-03-21     Completed Date:  2000-03-21     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  0375410     Medline TA:  J Pediatr     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  248-50     Citation Subset:  AIM; IM    
Affiliation:
Children's Hospital Oakland, Department of Hematology/Oncology, Oakland, CA 94609, USA.
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MeSH Terms
Descriptor/Qualifier:
Anemia, Neonatal / therapy*
Anemia, Sickle Cell / diagnosis*
Blood Group Incompatibility / therapy*
Child, Preschool
Erythrocyte Transfusion*
Humans
Infant
Infant, Newborn
Neonatal Screening*
Grant Support
ID/Acronym/Agency:
HL-20985/HL/NHLBI NIH HHS
Comments/Corrections
Comment In:
J Pediatr. 2000 Feb;136(2):145-6   [PMID:  10657816 ]

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


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