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Article

Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism.

Genes - 24 Nov 2021

Vick Philipp, Eberle Birgit, Choukair Daniela, Weiss Birgit, Roeth Ralph, Schneider Isabelle, Paramasivam Nagarajan, Bettendorf Markus, Rappold Gudrun A

Abstract excerpt

Congenital primary hypothyroidism (CH; OMIM 218700) is characterized by an impaired thyroid development, or dyshormonogenesis, and can lead to intellectual disability and growth retardation if untreated. Most of the children with congenital hypothyroidism present thyroid dysgenesis, a developmental anomaly of the thyroid. Various genes have been associated with thyroid dysgenesis, but all known genes together can...

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Identifiers

PMID: 34946811
DOI: 10.3390/genes12121862
PMCID: PMC8701029

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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