Challenges in the Diagnosis of Beta-thalassemia Syndrome: The Importance of Molecular Diagnosis

Patients with heterozygous β-thalassemia are generally asymptomatic. However, the intermediate phenotype is uncommon, and patients require further investigation to confirm the diagnosis. We describe a 32-year-old woman (gravida 3, para 2) with heterozygous β-thalassemia who presented with symptomati...

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Detalles Bibliográficos
Autores principales: Rameli, Nabilah, Ramli, Marini, Zulkafli, Zefarina, Hassan, Mohd Nazri, Yusoff, Shafini Mohd, Noor, Noor Haslina Mohd, Hussin, Suryati, Kamarudin, Nor Khairina Mohamed, Yusoff, Yuslina Mat, Bahar, Rosnah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: OMJ 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8804155/
https://www.ncbi.nlm.nih.gov/pubmed/35136660
http://dx.doi.org/10.5001/omj.2021.48

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8804155/
https://www.ncbi.nlm.nih.gov/pubmed/35136660
http://dx.doi.org/10.5001/omj.2021.48

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