Cargando…
Higher prevalence of permanent congenital hypothyroidism in the Southwest of Iran mostly caused by dyshormonogenesis: a five-year follow-up study
OBJECTIVE: The incidence of congenital hypothyroidism (CH) varies globally. This 5-year study aimed to determine the prevalence of permanent CH in the southwest of Iran. MATERIALS AND METHODS: Between January 2007 and December 2009, all newborns in Ahvaz, the biggest city in the southwest of Iran, w...
Autor principal: | Aminzadeh, Majid |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Endocrinologia e Metabologia
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10118670/ https://www.ncbi.nlm.nih.gov/pubmed/30624500 http://dx.doi.org/10.20945/2359-3997000000085 |
Ejemplares similares
-
High frequency of mutations in 'dyshormonogenesis genes' in severe congenital hypothyroidism
por: Makretskaya, Nina, et al.
Publicado: (2018) -
Prevalence of Permanent Congenital Hypothyroidism in Isfahan-Iran
por: Hashemipour, Mahin, et al.
Publicado: (2013) -
Prevalence of Permanent Congenital Hypothyroidism in Children in Yazd, Central Iran
por: ORDOOEI, Mahtab, et al.
Publicado: (2013) -
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)