Case Report: Functional Analysis and Neuropsychological Evaluation of Dyshormonogenetic Fetal Goiter in Siblings Caused by Novel Compound Hyterozygous TPO Gene Mutations

INTRODUCTION: It is rare for a euthyroid mother to carry a child with a fetal goiter. However, cases of congenital hypothyroidism (CH) caused by thyroid dyshormonogenesis have been reported. Even though gene mutations associated with fetal goiter have been reported in a few studies, the effects on i...

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Detalles Bibliográficos
Autores principales: Rodrigues, Tania Maria Barreto, Silva, Marlon Messias da Conceição, Freitas, Magali Maciel, Duarte, Zélia Maria Costa, Frutuoso, Vitória Sousa, Rodrigues, Mariana Teixeira, Rubio, Ileana Gabriela Sanchez
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8251258/
https://www.ncbi.nlm.nih.gov/pubmed/34220711
http://dx.doi.org/10.3389/fendo.2021.671659

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8251258/
https://www.ncbi.nlm.nih.gov/pubmed/34220711
http://dx.doi.org/10.3389/fendo.2021.671659

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