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)
| Descriptor ID |
D017042
|
| 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
- Maternal Phenylketonuria
- Phenylalanine-Hydroxylase Deficiency Disease, Maternal
- Phenylalanine Hydroxylase Deficiency Disease, Maternal
- PKU, Maternal
- Maternal Phenylalanine Hydroxylase Deficiency Disease
- Pregnancy in Phenylketonuria
- Phenylketonuria, Pregnancy in
|
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 this website by year, and whether "Phenylketonuria, Maternal" was a major or minor topic of these publications.
Below are the most recent publications written about "Phenylketonuria, Maternal" by people in Profiles.
-
Phenylketonuria and the brain. Mol Genet Metab. 2023 05; 139(1):107583.
-
Sapropterin dihydrochloride use in pregnant women with phenylketonuria: an interim report of the PKU MOMS sub-registry. Mol Genet Metab. 2014 May; 112(1):9-16.
-
Maternal Phenylketonuria International Collaborative Study revisited: evaluation of maternal nutritional risk factors besides phenylalanine for fetal congenital heart defects. J Inherit Metab Dis. 2014 Jan; 37(1):39-42.
-
Tetrahydrobiopterin and maternal PKU. Mol Genet Metab. 2005 Dec; 86 Suppl 1:S139-41.
-
MRI characterization of cerebral dysgenesis in maternal PKU. Acta Paediatr Suppl. 1994 Dec; 407:83-5.