Matches in SemOpenAlex for { <https://semopenalex.org/work/W1966166082> ?p ?o ?g. }
- W1966166082 endingPage "712" @default.
- W1966166082 startingPage "705" @default.
- W1966166082 abstract "Summary Malonic aciduria is a rare autosomal recessive disorder caused by deficiency of malonyl‐CoA decarboxylase, encoded by the MLYCD gene. We report on a patient with clinical presentation in the neonatal period. Metabolic investigations led to a diagnosis of malonyl‐CoA decarboxylase deficiency, confirmed by decreased activity in cultured fibroblasts. High doses of carnitine and a diet low in lipids led to a reduction in malonic acid excretion, and to an improvement in his clinical conditions, but at the age of 4 months he died suddenly and unexpectedly. No autopsy was performed. Molecular analysis of the MLYCD gene performed on the proband's RNA and genomic DNA identified a previously undescribed mutation (c.772–775delACTG) which was homozygous. This mutation was present in his mother but not in his father; paternity was confirmed by microsatellite analysis. A hypothesis of maternal uniparental disomy (UPD) was investigated using fourteen microsatellite markers on chromosome 16, and the results confirmed maternal UPD. Maternal isodisomy of the 16q24 region led to homozygosity for the MLYCD mutant allele, causing the patient's disease. These findings are relevant for genetic counselling of couples with a previously affected child, since the recurrence risk in future pregnancies is dramatically reduced by the finding of UPD. In addition, since the patient had none of the clinical manifestations previously associated with maternal UPD 16, this case provides no support for the existence of maternally imprinted genes on chromosome 16 with a major effect on phenotype." @default.
- W1966166082 created "2016-06-24" @default.
- W1966166082 creator A5004665891 @default.
- W1966166082 creator A5005055521 @default.
- W1966166082 creator A5020769869 @default.
- W1966166082 creator A5025732428 @default.
- W1966166082 creator A5033672223 @default.
- W1966166082 creator A5043038898 @default.
- W1966166082 creator A5051601800 @default.
- W1966166082 creator A5060693957 @default.
- W1966166082 creator A5066314417 @default.
- W1966166082 creator A5082595568 @default.
- W1966166082 date "2007-05-29" @default.
- W1966166082 modified "2023-09-30" @default.
- W1966166082 title "Fatal Malonyl CoA Decarboxylase Deficiency Due to Maternal Uniparental Isodisomy of the Telomeric End of Chromosome 16" @default.
- W1966166082 cites W1501129903 @default.
- W1966166082 cites W1796450910 @default.
- W1966166082 cites W1966348307 @default.
- W1966166082 cites W1971024458 @default.
- W1966166082 cites W1971168917 @default.
- W1966166082 cites W1973181474 @default.
- W1966166082 cites W1987400534 @default.
- W1966166082 cites W1990152592 @default.
- W1966166082 cites W1994437257 @default.
- W1966166082 cites W1994688667 @default.
- W1966166082 cites W1995006001 @default.
- W1966166082 cites W1997370697 @default.
- W1966166082 cites W2006042595 @default.
- W1966166082 cites W2006761046 @default.
- W1966166082 cites W2016563358 @default.
- W1966166082 cites W2020432769 @default.
- W1966166082 cites W2022414521 @default.
- W1966166082 cites W2030146959 @default.
- W1966166082 cites W2031846075 @default.
- W1966166082 cites W2033296726 @default.
- W1966166082 cites W2038881580 @default.
- W1966166082 cites W2047412657 @default.
- W1966166082 cites W2056467041 @default.
- W1966166082 cites W2063750325 @default.
- W1966166082 cites W2065894978 @default.
- W1966166082 cites W2072676874 @default.
- W1966166082 cites W2072830262 @default.
- W1966166082 cites W2089191991 @default.
- W1966166082 cites W2092729596 @default.
- W1966166082 cites W2101431784 @default.
- W1966166082 cites W2104479178 @default.
- W1966166082 cites W2113652000 @default.
- W1966166082 cites W2117931623 @default.
- W1966166082 cites W2119041499 @default.
- W1966166082 cites W2131413875 @default.
- W1966166082 cites W2138012016 @default.
- W1966166082 cites W2144252620 @default.
- W1966166082 cites W280251412 @default.
- W1966166082 cites W4249531782 @default.
- W1966166082 doi "https://doi.org/10.1111/j.1469-1809.2007.00373.x" @default.
- W1966166082 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17535268" @default.
- W1966166082 hasPublicationYear "2007" @default.
- W1966166082 type Work @default.
- W1966166082 sameAs 1966166082 @default.
- W1966166082 citedByCount "20" @default.
- W1966166082 countsByYear W19661660822012 @default.
- W1966166082 countsByYear W19661660822013 @default.
- W1966166082 countsByYear W19661660822015 @default.
- W1966166082 countsByYear W19661660822017 @default.
- W1966166082 countsByYear W19661660822018 @default.
- W1966166082 countsByYear W19661660822019 @default.
- W1966166082 countsByYear W19661660822021 @default.
- W1966166082 countsByYear W19661660822023 @default.
- W1966166082 crossrefType "journal-article" @default.
- W1966166082 hasAuthorship W1966166082A5004665891 @default.
- W1966166082 hasAuthorship W1966166082A5005055521 @default.
- W1966166082 hasAuthorship W1966166082A5020769869 @default.
- W1966166082 hasAuthorship W1966166082A5025732428 @default.
- W1966166082 hasAuthorship W1966166082A5033672223 @default.
- W1966166082 hasAuthorship W1966166082A5043038898 @default.
- W1966166082 hasAuthorship W1966166082A5051601800 @default.
- W1966166082 hasAuthorship W1966166082A5060693957 @default.
- W1966166082 hasAuthorship W1966166082A5066314417 @default.
- W1966166082 hasAuthorship W1966166082A5082595568 @default.
- W1966166082 hasConcept C104317684 @default.
- W1966166082 hasConcept C126322002 @default.
- W1966166082 hasConcept C134018914 @default.
- W1966166082 hasConcept C150194340 @default.
- W1966166082 hasConcept C180754005 @default.
- W1966166082 hasConcept C188997412 @default.
- W1966166082 hasConcept C190727270 @default.
- W1966166082 hasConcept C201492766 @default.
- W1966166082 hasConcept C2780332060 @default.
- W1966166082 hasConcept C30481170 @default.
- W1966166082 hasConcept C501734568 @default.
- W1966166082 hasConcept C53226629 @default.
- W1966166082 hasConcept C54355233 @default.
- W1966166082 hasConcept C71924100 @default.
- W1966166082 hasConcept C86803240 @default.
- W1966166082 hasConceptScore W1966166082C104317684 @default.
- W1966166082 hasConceptScore W1966166082C126322002 @default.
- W1966166082 hasConceptScore W1966166082C134018914 @default.
- W1966166082 hasConceptScore W1966166082C150194340 @default.