Article

Mutation screening of eight genes and comparison of the clinical data in a Chinese cohort with congenital hypothyroidism

2022-05-04

Abstract excerpt

<h4>Background: </h4> Congenital hypothyroidism (CH) is a common neonatal endocrine disorder, characterized by irreversible intellectual disability and short stature if left untreated. It can be divided into thyroid dysgenesis (TD), including athyreosis, ectopy and hypoplasia, and dyshormonogenesis (DH), also referring to gland in situ (GIS), in which patients have eutopic thyroids with normal size or goiter. This...

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Literature Corpus work: 07d79e25-fd32-57d0-9437-9c0af62d5027
DOI: 10.21203/rs.3.rs-1603128/v1

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