Clinical Trial: TG Gene Mutations and Congenital Hypothyroidism

Study Status: Completed
Recruit Status: Completed
Study Type: Observational




Official Title: Congenital Hypothyroidism Due to Thyroglobulin Mutations in an Inbred Brazilian Family: A Novel Compound Heterozygous Constellation and Intronic Mutation Related to Fetal

Brief Summary: The aim of this study was to identify mutations in the thyroglobulin gene that might be present in patients with fetal goiter and congenital goiter hypothyroidism.