Further Evidence That Defects in Main Thyroid Dysgenesis-Related Genes Are an Uncommon Etiology for Primary Congenital Hypothyroidism in Mexican Patients: Report of Rare Variants in
FOXE1
Mexican population
NKX2-1
NKX2-5
PAX8
TSH receptor
congenital hypothyroidism
multiplex ligation-dependent probe amplification (MLPA)
polyalanine tract
protein modeling
thyroid dysgenesis
Journal
Children (Basel, Switzerland)
ISSN: 2227-9067
Titre abrégé: Children (Basel)
Pays: Switzerland
ID NLM: 101648936
Informations de publication
Date de publication:
30 May 2021
30 May 2021
Historique:
received:
16
04
2021
revised:
26
05
2021
accepted:
27
05
2021
entrez:
2
6
2021
pubmed:
3
6
2021
medline:
3
6
2021
Statut:
epublish
Résumé
Mexico shows a high birth prevalence of congenital hypothyroidism (CH) due to thyroid dysgenesis (TD).
Identifiants
pubmed: 34070861
pii: children8060457
doi: 10.3390/children8060457
pmc: PMC8227333
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Fondo Sectorial de Investigación en Salud y Seguridad Social SS/IMSS/ISSSTE-CONACyT
ID : SALUD-2014-01-233654
Organisme : Instituto Nacional de Pediatria
ID : Recursos Fiscales 2015-2020, Programa E022 Investigación y Desarrollo Tecnológico en Salud
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