[HTML][HTML] Thalassemia: A Review of the Challenges to the Families and Caregivers
R Yousuf, S Akter, SM Wasek, S Sinha, R Ahmad… - Cureus, 2022 - ncbi.nlm.nih.gov
Thalassemias are a group of congenital hemoglobin (Hb) disorders distinguished by
dwindling or total curtailment of production of one or more globin chains of hemoglobin …
dwindling or total curtailment of production of one or more globin chains of hemoglobin …
Epidemiology of clinically significant forms of alpha‐and beta‐thalassemia: A global map of evidence and gaps
KM Musallam, L Lombard, KD Kistler… - American journal of …, 2023 - Wiley Online Library
This systematic literature review assessed the global prevalence and birth prevalence of
clinically significant forms of alpha‐and beta‐thalassemia. Embase, MEDLINE, and the …
clinically significant forms of alpha‐and beta‐thalassemia. Embase, MEDLINE, and the …
[PDF][PDF] Knowledge, Attitudes, and Perceptions Towards Beta-Thalassemia among Residents of Azad Kashmir, Pakistan
F Shafique, S Ali, M ul Hassan… - Punjab University Journal …, 2023 - researchgate.net
β-Thalassemia is the most common genetic disorder of the time. In Pakistan, around 1–4 per
1000 infants is diagnosed with the disease making it one of the high-risk countries in the …
1000 infants is diagnosed with the disease making it one of the high-risk countries in the …
Improving the diagnosis of under-recognized, rare diseases in Asian populations: Systematic analysis of rare disease databases
D Ih, K Amaral, H Shi, A Jamal… - Journal of Asian …, 2024 - journalofasianhealth.org
Rare diseases affect approximately 30 million Americans, but fewer than one in 10 of these
patients receive an accurate diagnosis and timely, appropriate treatment. Many of these …
patients receive an accurate diagnosis and timely, appropriate treatment. Many of these …
[PDF][PDF] Investigation of the Serotonin, Cortisol Hormones and some Biochemical Parameters in Patients with Beta Thalassemia in Thi-Qar Governorate/Iraq
Beta thalassemia (β-thalassemia) is the most severe kind of β-thalassemia hereditary
disease that makes blood transfusion dependent. Patients with β-thalassemia disease …
disease that makes blood transfusion dependent. Patients with β-thalassemia disease …
Thalassemia: A Review of the Challenges to the Families and Caregivers
Y Rabeya, A Shaima, SM Wasek, S Susmita… - Cureus, 2022 - search.proquest.com
Thalassemias are a group of congenital hemoglobin (Hb) disorders distinguished by
dwindling or total curtailment of production of one or more globin chains of hemoglobin …
dwindling or total curtailment of production of one or more globin chains of hemoglobin …
Study on Clinical Features, Detection of Risk Factors and Causes of Anaemia in Children in a Tertiary Care Hospital of Bangladesh
N Paul, MR Islam, N Nusrat - Bangladesh Journal of Child Health, 2023 - banglajol.info
Background: Anaemia is a common childhood health problem. Among the causes of
anaemia besides the nutritional anaemia congenital hemoglobin disorder such as …
anaemia besides the nutritional anaemia congenital hemoglobin disorder such as …