Cargando…
Frequency of unnecessary prenatal diagnosis of hemoglobinopathies: A large retrospective analysis and implication to improvement of the control program
OBJECTIVE: To determine the frequency and etiology of unnecessary prenatal diagnosis for hemoglobinopathies during 12 years of services at a single university center in Thailand. METHODS: We conducted a retrospective cohort analysis of prenatal diagnosis during 2009–2021. A total of 4,932 couples at...
Autores principales: | Singha, Kritsada, Yamsri, Supawadee, Chaibunruang, Attawut, Srivorakun, Hataichanok, Sanchaisuriya, Kanokwan, Fucharoen, Goonnapa, Fucharoen, Supan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104333/ https://www.ncbi.nlm.nih.gov/pubmed/37058522 http://dx.doi.org/10.1371/journal.pone.0283051 |
Ejemplares similares
-
Diagnostic value of fetal hemoglobin Bart’s for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy
por: Singha, Kritsada, et al.
Publicado: (2022) -
A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration
por: Srivorakun, Hataichanok, et al.
Publicado: (2014) -
Evaluation of staff performance and interpretation of the screening program for prevention of thalassemia
por: Prommetta, Simaporn, et al.
Publicado: (2017) -
Anemia in an ethnic minority group in lower northern Thailand: A community-based study investigating the prevalence in relation to inherited hemoglobin disorders and iron deficiency
por: Pyae, Thinzar Win, et al.
Publicado: (2023) -
Thalassemia and erythroid transcription factor KLF1 mutations associated with borderline hemoglobin A(2) in the Thai population
por: Srivorakun, Hataichanok, et al.
Publicado: (2020)