succinylacetone has been researched along with Pregnancy in 11 studies
succinylacetone: inhibitor of heme biosynthesis
4,6-dioxoheptanoic acid : A dioxo monocarboxylic acid that is heptanoic acid in which oxo groups replace the hydrogens at positions 4 and 6. It is an abnormal metabolite of the tyrosine metabolic pathway and a marker for type 1 tyrosinaemia.
Pregnancy: The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH.
| Excerpt | Relevance | Reference |
|---|---|---|
| " During her pregnancy she was treated with diet (prescribed tyrosine intake 300 mg/day), and nitisinone (60 mg/day)." | 3.76 | Maternal and fetal tyrosinemia type I. ( Benoist, JF; Davit-Spraul, A; Garcia Segarra, N; Grenèche, MO; Imbard, A; Ogier de Baulny, H; Roche, S, 2010) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (63.64) | 18.7374 |
| 1990's | 3 (27.27) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (9.09) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Garcia Segarra, N | 1 |
| Roche, S | 1 |
| Imbard, A | 1 |
| Benoist, JF | 1 |
| Grenèche, MO | 1 |
| Davit-Spraul, A | 1 |
| Ogier de Baulny, H | 1 |
| King, GS | 2 |
| MacKenzie, F | 2 |
| Pettit, BR | 3 |
| Leonard, JV | 2 |
| Steinmann, B | 1 |
| Gitzelmann, R | 1 |
| Kvittingen, EA | 4 |
| Stokke, O | 1 |
| Gagné, R | 2 |
| Lescault, A | 1 |
| Grenier, A | 2 |
| Laberge, C | 2 |
| Mélançon, SB | 1 |
| Dallaire, L | 1 |
| Cederbaum, S | 1 |
| Jakobs, C | 3 |
| Tanguay, RM | 2 |
| Poudrier, J | 1 |
| Lettre, F | 1 |
| St-Louis, M | 1 |
| Stellaard, F | 1 |
| Henderson, M | 1 |
| Lilford, R | 1 |
| Dorland, L | 1 |
| Wikkerink, B | 1 |
| Kok, RM | 1 |
| de Jong, AP | 1 |
| Wadman, SK | 1 |
| Brodtkorb, E | 1 |
11 other studies available for succinylacetone and Pregnancy
| Article | Year |
|---|---|
Maternal and fetal tyrosinemia type I.
Topics: Biomarkers; Child Development; Consanguinity; Cyclohexanones; Diet, Protein-Restricted; DNA Mutation | 2010 |
Neonatal and prenatal diagnosis of hereditary tyrosinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Female; Heptanoates; Humans; Hydrolases; Infan | 1983 |
The antenatal diagnosis and aid to the management of hereditary tyrosinaemia by use of a specific and sensitive GC-MS assay for succinylacetone.
Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Female; Gas Chromatography-Mass Spectrometry; | 1984 |
Prenatal diagnosis of hereditary tyrosinemia.
Topics: Amino Acid Metabolism, Inborn Errors; Amniocentesis; Female; Heptanoates; Humans; Infant, Newborn; P | 1984 |
Prenatal diagnosis of hereditary tyrosinaemia: measurement of succinylacetone in amniotic fluid.
Topics: Amniotic Fluid; Female; Genes, Recessive; Heptanoates; Heptanoic Acids; Humans; Hydrolases; Liver; M | 1982 |
A case of tyrosinaemia type I with normal level of succinylacetone in the amniotic fluid.
Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Cells, Cultured; DNA Mutational Analysis; Enzy | 1996 |
Genotyping of a case of tyrosinaemia type I with normal level of succinylacetone in amniotic fluid.
Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Female; Genotype; Heptanoates; Heterozygote; H | 1999 |
First-trimester prenatal diagnosis of tyrosinemia type I by amniotic fluid succinylacetone determination.
Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Female; Heptanoates; Heptanoic Acids; Humans; | 1990 |
Early prenatal diagnosis of hereditary tyrosinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Female; Heptanoates; Humans; Pregnancy; Pregna | 1985 |
Stable isotope dilution analysis of succinylacetone using electron capture negative ion mass fragmentography: an accurate approach to the pre- and neonatal diagnosis of hereditary tyrosinemia type I.
Topics: Amino Acid Metabolism, Inborn Errors; Electrons; Female; Gas Chromatography-Mass Spectrometry; Hepta | 1988 |
The pre- and post-natal diagnosis of tyrosinemia type I and the detection of the carrier state by assay of fumarylacetoacetase.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Child; Female; Genetic Carrier Screening; Genetic Varia | 1986 |