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Pregnancy in women heterozygous for MCT8 mutations: risk of maternal hypothyroxinemia and fetal care
Autor:
Nathalie Neri, Jeanne Amiel, Aurore Carré, Laurent Mandelbrot, Elodie Tron, Michel Polak, Helton Estrela Ramos, Albane Simon, Vassili Valayannopoulos, Isabelle Desguerre, Jean-Paul Bonnefont, Corinne Floch, Melina Morandini, Benoit De Sarcus, Mireille Castanet
Publikováno v:
European Journal of Endocrinology. 164:309-314
ContextMonocarboxylate transporter 8 (MCT8 or SLC16A2) mutations cause X-linked Allan–Herndon–Dudley syndrome. Heterozygous females are usually asymptomatic, but pregnancy may modify thyroid function and MCT8 is expressed in the placenta, suggest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76d6253b2ec09527fe585e8c22f23d31
https://doi.org/10.1530/eje-10-0679
https://doi.org/10.1530/eje-10-0679
