Ontology highlight
ABSTRACT:
SUBMITTER: Randon DN
PROVIDER: S-EPMC7380325 | biostudies-literature | 2020 Jul
REPOSITORIES: biostudies-literature
Randon Dévora N DN Sperb-Ludwig Fernanda F Vianna Fernanda S L FSL Becker Ana P P APP Vargas Carmen R CR Sitta Angela A Sant'Ana Alexia N AN Schwartz Ida V D IVD Bitencourt Fernanda H de FH
Genetics and molecular biology 20200724 3
Citrullinemia type 1 (CTLNI), long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD), and mut0 methylmalonic acidemia (mut0 MMA) are inborn errors of metabolism (IEMs) associated with sudden unexpected death in infancy (SUDI). Its most common pathogenic variants are: c.1168G>A (CTLNI, ASS1 gene), c.1528G>C (LCHADD, HADHA gene), c.655A>T and c.1106G>A (mut0 MMA, MUT gene). Considering the absence of estimates regarding the incidence of these diseases in Brazil, this study soug ...[more]