Document Detail


Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension of the newborn.
MedLine Citation:
PMID:  10753260     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Congenital dyserythropoietic anemia (CDA) is a rare group of inherited bone marrow disorders characterized by anemia with ineffective erythropoiesis. We report 3 siblings from a family known to have CDA type I who presented with persistent pulmonary hypertension of the newborn (PPHN). We suggest that the diagnosis of CDA type I should be considered in any neonate with PPHN and anemia.
Authors:
H Shalev; A Moser; J Kapelushnik; M Karplus; N Zucker; I Yaniv; H Tamary
Publication Detail:
Type:  Case Reports; Journal Article; Review    
Journal Detail:
Title:  The Journal of pediatrics     Volume:  136     ISSN:  0022-3476     ISO Abbreviation:  J. Pediatr.     Publication Date:  2000 Apr 
Date Detail:
Created Date:  2000-05-03     Completed Date:  2000-05-03     Revised Date:  2005-11-16    
Medline Journal Info:
Nlm Unique ID:  0375410     Medline TA:  J Pediatr     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  553-5     Citation Subset:  AIM; IM    
Affiliation:
Division of Pediatrics, Soroka Medical Center, Beer Sheva, Israel.
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MeSH Terms
Descriptor/Qualifier:
Anemia, Dyserythropoietic, Congenital / diagnosis*,  genetics
Arabs
Consanguinity
Diagnosis, Differential
Female
Humans
Infant, Newborn
Israel
Male
Pedigree
Persistent Fetal Circulation Syndrome / diagnosis*,  genetics

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


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