دورية أكاديمية

Asymptomatic hemochromatosis case with HFE c.1007−47G>A, c.340+4T>C heterozygous mutations and alpha globin −3.7 kb deletion

التفاصيل البيبلوغرافية
العنوان: Asymptomatic hemochromatosis case with HFE c.1007−47G>A, c.340+4T>C heterozygous mutations and alpha globin −3.7 kb deletion
المؤلفون: Akar, Nejat, Çelik, Vesile Deniz, Kılıç, Betül Orhan, ArdıçoÄŸlu Akışın, Nazife Yasemin
سنة النشر: 2019
مصطلحات موضوعية: Hemochromatosis, HFE gene mutation, Alpha globulin deletion
الوصف: Background Hereditary hemochromatosis is a disease associated with iron deposition which is caused by the mutations in “hereditary Fe (iron)†(HFE) gene. Case The 16-year-old male patient was diagnosed with hereditary hemochromatosis after c.1007?47G>A heterozygous c.340+4?T>C heterozygous mutations were detected in HFE gene analysis after a suspicion of hemochromatosis due to increase of hemoglobin value from 14.8?g/dL to 16.8?g/dL and the level of ferritin from 68?ng/ml to 300?ng/ml in routine check-up controls in two-years period. In addition, due to low mean corpuscular volume (MCV) (76?fL), and mean corpuscular hemoglobin (MCH) (26?pg) levels, gene mutation analysis was carried out and the patient was also shown to carry ? thalassemia ?3.7 deletions. Conclusion Early diagnosis of hemochromatosis is important in terms of prognosis and morbidity. We aimed to emphasize that we can easily diagnose the disease by performing genetic analysis in cases with suspected hemochromatosis even they have no complaints.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: Egyptian Journal of Medical Human Genetics; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; 110-8630; https://doi.org/10.1016/j.ejmhg.2018.06.001Test; https://hdl.handle.net/20.500.11851/3219Test; https://www.sciencedirect.com/science/article/pii/S1110863018300685Test; 19; 433; 435; 2-s2.0-85053318522; Q4
DOI: 10.1016/j.ejmhg.2018.06.001
الإتاحة: https://doi.org/20.500.11851/321910.1016/j.ejmhg.2018.06.001Test
https://hdl.handle.net/20.500.11851/3219Test
https://www.sciencedirect.com/science/article/pii/S1110863018300685Test
حقوق: open
رقم الانضمام: edsbas.B9034FC2
قاعدة البيانات: BASE