Services like antenatal diagnosis for six common mutations for thalassemia and sickle cell mutation analysis will also be done here." ...

Prevention of thalassemia is crucial. If a family member is diagnosed, it is vital that all siblings undergo screening. Marriages between gene carriers should be avoided, or if such unions occur, ...

Transfusion-dependent β-thalassemia (TDT) patients in France face significant health care demands and clinical challenges, with frequent complications and high mortality rates. Patients with TDT ...

Background Understanding patients' views about medication is crucial to maximize adherence. Thalassemia is a congenital blood disorder requiring chronic blood transfusions and daily iron chelation ...

For the freshest news, join The Borneo Post's Telegram Channel and The Borneo Post on Newswav. Previous ArticleMinimum wage: Sabah timber industries call for moratorium ...

Twenty-five controls, including children with sickle-cell trait and Hgb SC and Hgb S-β thalassemia diseases, regularly demonstrated splenic uptake. Functional asplenia in children with sickle ...

According to the draft received by “Jang,” the bill aims to establish an effective system where the people of Punjab will have access to both genetic counseling and thalassemia diagnosis services.

This study has many strengths and is the first study of beliefs in medications in thalassemia. We were able to analyze a large, racially diverse, international sample of thalassemia patients ...

It was the same with Indian actress Alia Bhatt, who while sharing her ADHD diagnosis, said that she used to “get zoned out from a young age”. She is not the only famous person with this condition, ...

Public sector hospitals in India face a critical shortage of Desferal, a vital iron chelator, endangering thalassemia patients who cannot afford its high cost. Listen to Story Public hospitals face an ...