Document Detail


Cobalamin and folate deficiency: acquired and hereditary disorders in children.
MedLine Citation:
PMID:  9930566     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
This review highlights the features of cobalamin and folate deficiency and insufficiency that are particular to children. Maternal deficiency of cobalamin and insufficiency or deficiency of folate are the principal causes of deficiencies of these vitamins in the newborn. Maternal cobalamin deficiency can be caused by pernicious anemia or postgastrectomy, but most often results from a diet lacking in animal protein. The mothers are usually not anemic and failure to thrive and neurological deficits are more common in their infants than is megaloblastic anemia. Inborn errors of cobalamin transport and metabolism present with homocystinuria and methylmalonic aciduria, either alone or in combination. They share many of the clinical features of nutritional cobalamin deficiency. Maternal folate insufficiency results in neural tube defects, fetal loss, prematurity, and fetal growth retardation. Inborn errors of folate metabolism are rare, but polymorphisms affecting the gene for methylenetetrahydrofolate reductase (MTHFR) are common and may have significant health implications. Elevation of plasma methylmalonic acid (MMA) levels reflects a functional lack of cobalamin, whereas elevated total homocysteine levels are associated with a lack of either folate or cobalamin. The determination of these should be part of the investigation of failure to thrive, neurological disorders, and unexplained anemia or cytopenias in children.
Authors:
D S Rosenblatt; V M Whitehead
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review    
Journal Detail:
Title:  Seminars in hematology     Volume:  36     ISSN:  0037-1963     ISO Abbreviation:  Semin. Hematol.     Publication Date:  1999 Jan 
Date Detail:
Created Date:  1999-03-18     Completed Date:  1999-03-18     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0404514     Medline TA:  Semin Hematol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  19-34     Citation Subset:  IM    
Affiliation:
Faculty of Medicine, McGill University, The Royal Victoria and Montreal General Hospitals, QC, Canada.
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MeSH Terms
Descriptor/Qualifier:
Diet
Female
Folic Acid Deficiency / etiology*,  genetics
Humans
Infant
Infant, Newborn
Maternal-Fetal Exchange
Metabolism, Inborn Errors
Pregnancy
Vitamin B 12 Deficiency / etiology*,  genetics

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


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