Phenylketonuria, Maternal
"Phenylketonuria, Maternal" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A condition occurring in untreated or partially treated females with PHENYLKETONURIA when they become pregnant. This may result in damages to the FETUS, including MICROCEPHALY; MENTAL RETARDATION; congenital heart disease; FETAL GROWTH RETARDATION; and CRANIOFACIAL ABNORMALITIES. (From Am J Med Genet 1997 Mar 3;69(1):89-95)
MeSH Number(s)
C10.228.140.163.100.687.500
C13.703.575
C16.320.565.100.766.500
C16.320.565.189.687.500
C18.452.132.100.687.500
C18.452.648.100.766.500
C18.452.648.189.687.500
Concept/Terms
Phenylketonuria, Maternal- Phenylketonuria, Maternal
- PKU, Maternal
- Pregnancy in Phenylketonuria
- Phenylketonuria, Pregnancy in
- Phenylketonurias, Pregnancy in
- Pregnancy in Phenylketonurias
- in Phenylketonuria, Pregnancy
- in Phenylketonurias, Pregnancy
- Phenylalanine-Hydroxylase Deficiency Disease, Maternal
- Maternal Phenylketonuria
- Maternal Phenylalanine Hydroxylase Deficiency Disease
Below are MeSH descriptors whose meaning is more general than "Phenylketonuria, Maternal".
- Diseases [C]
- Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
- Brain Diseases [C10.228.140]
- Brain Diseases, Metabolic [C10.228.140.163]
- Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
- Phenylketonurias [C10.228.140.163.100.687]
- Phenylketonuria, Maternal [C10.228.140.163.100.687.500]
- Female Urogenital Diseases and Pregnancy Complications [C13]
- Pregnancy Complications [C13.703]
- Phenylketonuria, Maternal [C13.703.575]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Metabolism, Inborn Errors [C16.320.565]
- Amino Acid Metabolism, Inborn Errors [C16.320.565.100]
- Phenylketonurias [C16.320.565.100.766]
- Phenylketonuria, Maternal [C16.320.565.100.766.500]
- Brain Diseases, Metabolic, Inborn [C16.320.565.189]
- Phenylketonurias [C16.320.565.189.687]
- Phenylketonuria, Maternal [C16.320.565.189.687.500]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Brain Diseases, Metabolic [C18.452.132]
- Brain Diseases, Metabolic, Inborn [C18.452.132.100]
- Phenylketonurias [C18.452.132.100.687]
- Phenylketonuria, Maternal [C18.452.132.100.687.500]
- Metabolism, Inborn Errors [C18.452.648]
- Amino Acid Metabolism, Inborn Errors [C18.452.648.100]
- Phenylketonurias [C18.452.648.100.766]
- Phenylketonuria, Maternal [C18.452.648.100.766.500]
- Brain Diseases, Metabolic, Inborn [C18.452.648.189]
- Phenylketonurias [C18.452.648.189.687]
- Phenylketonuria, Maternal [C18.452.648.189.687.500]
Below are MeSH descriptors whose meaning is more specific than "Phenylketonuria, Maternal".
This graph shows the total number of publications written about "Phenylketonuria, Maternal" by people in Harvard Catalyst Profiles by year, and whether "Phenylketonuria, Maternal" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 1 | 0 | 1 |
| 1997 | 1 | 0 | 1 |
| 1998 | 1 | 0 | 1 |
| 1999 | 1 | 0 | 1 |
| 2000 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2003 | 5 | 1 | 6 |
| 2012 | 1 | 0 | 1 |
Below are the most recent publications written about "Phenylketonuria, Maternal" by people in Profiles.
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Congenital heart disease in maternal PKU. Mol Genet Metab. 2012 Dec; 107(4):648-9.
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Research design, organization, and sample characteristics of the Maternal PKU Collaborative Study. Pediatrics. 2003 Dec; 112(6 Pt 2):1519-22.
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The Maternal Phenylketonuria International Study: 1984-2002. Pediatrics. 2003 Dec; 112(6 Pt 2):1523-9.
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Pregnancy experiences in the woman with mild hyperphenylalaninemia. Pediatrics. 2003 Dec; 112(6 Pt 2):1548-52.
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Cognitive and behavioral development in maternal phenylketonuria offspring. Pediatrics. 2003 Dec; 112(6 Pt 2):1544-7.
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Impact of the phenylalanine hydroxylase gene on maternal phenylketonuria outcome. Pediatrics. 2003 Dec; 112(6 Pt 2):1530-3.
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Historical background for the maternal PKU syndrome. Pediatrics. 2003 Dec; 112(6 Pt 2):1516-8.
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Barriers to successful dietary control among pregnant women with phenylketonuria. Genet Med. 2002 Mar-Apr; 4(2):84-9.
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The International Collaborative Study of Maternal Phenylketonuria: status report 1998. Eur J Pediatr. 2000 Oct; 159 Suppl 2:S156-60.
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The Resource Mothers Program for Maternal Phenylketonuria. Am J Public Health. 1999 May; 89(5):762-4.