Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Congenital hypothyroidism].

Annales d'endocrinologie - 1 Sept 2006

Carranza D, Van Vliet G, Polak M

Abstract excerpt

Congenital hypothyroidism is the principle cause of preventable mental retardation, with a prevalence of 1 in 3,500 neonates. The disorder may be permanent or transitory. Permanent congenital hypothyroidism is caused principally by thyroid dysgenesis. In industrialized countries, mass screening a...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Intellectual Disability
Share to Mutation
Share to Sex Characteristics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Newborn

Share to PAX8 gene

Share to Hypothyroidism

Source

Identifiers

PMID: 17072233
DOI: 10.1016/s0003-4266(06)72601-4

Genes

PAX8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17072233-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Congenital hypothyroidism].PMID 17072233Read ↗

[Molecular-genetic aspects of congenital hypothyroidism].Semantic proximity Read ↗

[Congenital hypothyroidism].Semantic proximity Read ↗

Congenital hypothyroidism: etiologies, diagnosis, and management.Semantic proximity Read ↗

[Genetic of congenital hypothyroidism].Semantic proximity Read ↗

Detection and treatment of congenital hypothyroidism.Semantic proximity Read ↗

Heterogeneous phenotype in children affected by non-autoimmune hypothyroidism: an update.Semantic proximity Read ↗

Genetics of congenital hypothyroidism.Semantic proximity Read ↗

Genetics of congenital hypothyroidism: Modern conceptsSemantic proximity Read ↗

Extrathyroidal congenital defects in children with congenital hypothyroidism - observations from a single paediatric centre in Central Europe with a review of literature.Semantic proximity Read ↗

[Neonatal hypothyroidism].Semantic proximity Read ↗

Thyroglobulin gene mutations and other genetic defects associated with congenital hypothyroidism.Semantic proximity Read ↗

Neonatal thyroid disorders.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.