Cargando…
Genetic Factors Causing Thyroid Dyshormonogenesis as the Major Etiologies for Primary Congenital Hypothyroidism: Clinical and Genetic Characterization of 33 Patients
Background and aims: Although the significance of primary congenital hypothyroidism (CH) is supported by an increasing amount of evidence, the clinical and genetic characteristics of this condition are still poorly understood. This study aimed to explore the underlying genetic etiologies in a cohort...
Autores principales: | Liu, Rui, Tian, Jing-Li, Huang, Xiao-Ling, Song, Yuan-Zong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9786654/ https://www.ncbi.nlm.nih.gov/pubmed/36555929 http://dx.doi.org/10.3390/jcm11247313 |
Ejemplares similares
-
High frequency of mutations in 'dyshormonogenesis genes' in severe congenital hypothyroidism
por: Makretskaya, Nina, et al.
Publicado: (2018) -
Molecular Genetic Characterization of Thyroid Dyshormonogenesis in a French Bulldog
por: Major, S., et al.
Publicado: (2015) -
Next-Generation Sequencing Analysis Reveals Frequent Familial Origin and Oligogenism in Congenital Hypothyroidism With Dyshormonogenesis
por: Oliver-Petit, Isabelle, et al.
Publicado: (2021) -
Analysis of the T354P mutation of the sodium/iodide cotransporter gene in children with congenital hypothyroidism due to dyshormonogenesis
por: Miranzadeh-Mahabadi, Hajar, et al.
Publicado: (2016) -
Higher prevalence of permanent congenital hypothyroidism in the Southwest of Iran mostly caused by dyshormonogenesis: a five-year follow-up study
por: Aminzadeh, Majid
Publicado: (2018)