The Resource Mothers Program for Maternal Phenylketonuria.
- 1 May 1999
- journal article
- clinical trial
- Published by American Public Health Association in American Journal of Public Health
- Vol. 89 (5) , 762-764
- https://doi.org/10.2105/ajph.89.5.762
Abstract
OBJECTIVES: The purpose of this study was to measure the effectiveness of resource mothers in reducing adverse consequences of maternal phenylketonuria. METHODS: Nineteen pregnancies in the resource mothers group were compared with 64 pregnancies in phenylketonuric women without resource mothers. Weeks to metabolic control and offspring outcome were measured. RESULTS: Mean number of weeks to metabolic control was 8.5 (SE = 2.2) in the resource mothers group, as compared with 16.1 (SE = 1.7) in the comparison group. Infants of women in the resource mothers group had larger birth head circumferences and higher developmental quotients. CONCLUSIONS: The resource mothers program described here improves metabolic control in pregnant women with phenylketonuria.Keywords
This publication has 11 references indexed in Scilit:
- The international collaborative study on maternal phenylketonuria: organization, study design and description of the sampleEuropean Journal of Pediatrics, 1996
- Psychosocial factors in maternal phenylketonuria: women's adherence to medical recommendations.American Journal of Public Health, 1995
- The international collaborative study of maternal phenylketonuria: status report 1994Acta Paediatrica, 1994
- Personality disorder in young women with treated phenylketonuriaJournal of Inherited Metabolic Disease, 1994
- An Update of the Swedish Reference Standards for Weight, Length and Head Circumference at Birth for Given Gestational Age (1977‐1981)Acta Paediatrica, 1991
- TIMING OF STRICT DIET IN RELATION TO FETAL DAMAGE IN MATERNAL PHENYLKETONURIAThe Lancet, 1987
- Maternal phenylketonuria (PKU) — A reviewClinical Biochemistry, 1987
- Diet policies of PKU clinics in the United States.American Journal of Public Health, 1984
- Maternal Phenylketonuria and HyperphenylalaninemiaNew England Journal of Medicine, 1980