Document Detail

Maternal phenylketonuria (PKU)--a review.
MedLine Citation:
PMID:  3308176     Owner:  NLM     Status:  MEDLINE    
This review points out the very high incidence of damage to the fetus in untreated maternal phenylketonuria (PKU). In classical cases, 92% of the offspring are mentally retarded, 73% have microcephaly, 40% are growth retarded at birth, and 12% have congenital anomalies. Less severe types of PKU and its variants and patients treated with a low phenylalanine diet during pregnancy have a much lower incidence of these defects in their offspring. Very promising results have been obtained in a small number of preconception and early first trimester treated patients under very strict dietary control. Nutrition of the mother and fetus is a major concern during the application of this restrictive diet and must be monitored closely to avoid fetal damage from malnutrition. A 7-year collaborative study of maternal PKU began in November 1984 in the US and Canada, but even in this well publicized study, many patients are presenting late for treatment. It is suggested that premarital and/or prenatal screening for maternal PKU should be initiated for the next generation.
W B Hanley; J T Clarke; W Schoonheyt
Related Documents :
10371756 - Cytoplasmic factors do not contribute to a maternal effect on ethanol teratogenesis.
23152876 - High fat diet induced developmental defects in the mouse: oocyte meiotic aneuploidy and...
20102736 - Maternal methadone dose during pregnancy and infant clinical outcome.
11509096 - Nutrition and maternal morbidity and mortality.
22604746 - Pathological cases of the month: case 1.
8215826 - Chronic intervillositis of the placenta.
Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  Clinical biochemistry     Volume:  20     ISSN:  0009-9120     ISO Abbreviation:  Clin. Biochem.     Publication Date:  1987 Jun 
Date Detail:
Created Date:  1987-10-27     Completed Date:  1987-10-27     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  0133660     Medline TA:  Clin Biochem     Country:  CANADA    
Other Details:
Languages:  eng     Pagination:  149-56     Citation Subset:  IM    
Department of Paediatrics, Hospital for Sick Children, Toronto, Ontario, Canada.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Congenital Abnormalities / etiology*
Fetal Diseases / etiology
Pregnancy Complications*

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

Previous Document:  Development of coronary artery disease in cardiac transplant patients receiving immunosuppressive th...
Next Document:  Pitfalls in the initial diagnosis of tyrosinemia: three case reports and a review of the literature.