Cargando…
A novel compound heterozygous of β-thalassemia with HbG-Coushatta: case report of Iran
A 30-year-old male couple from Ardabil city, Iran, were admitted for premarital screening. An abnormal band in HbS/D regions with high levels of HbF and HbA 2 led us to suspect the possibility of a compound heterozygous state of β-thalassemia in our affected proband. Therefore, beta globin chain seq...
Autores principales: | Soozangar, Narges, Abbaspour, Ehsan, Mokaber, Haleh, Nematollahi, Zahra, Davarnia, Behzad |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10185494/ https://www.ncbi.nlm.nih.gov/pubmed/37188672 http://dx.doi.org/10.1038/s41439-023-00243-y |
Ejemplares similares
-
GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran
por: Abbaspour Rodbaneh, Ehsan, et al.
Publicado: (2021) -
Association of polymorphisms in the HBG1‐HBD intergenic region with HbF levels
por: Hu, Li, et al.
Publicado: (2020) -
The compound state: Hb S/beta-thalassemia()
por: Figueiredo, Maria Stella
Publicado: (2015) -
Estimating the age of Hb G‐Coushatta [β22(B4)Glu→Ala] mutation by haplotypes of β‐globin gene cluster in Denizli, Turkey
por: Ozturk, Onur, et al.
Publicado: (2018) -
HBG2 -158 (C>T) polymorphism and its contribution to fetal hemoglobin variability in Iraqi Kurds with beta-thalassemia minor
por: Albarawi, Dilan J., et al.
Publicado: (2018)