[HTML][HTML] Infection and potential challenge of childhood mortality in sickle cell disease: a comprehensive review of the literature from a global perspective
Sickle cell disease (SCD) is a complex genetic disorder associated with multiple clinical
manifestations, including increased susceptibility to bacterial and viral infections. This …
manifestations, including increased susceptibility to bacterial and viral infections. This …
Myopia in India
India is a culturally and geographically diverse nation. Its vast demographic nature does not
allow a single definition for any of the given medical conditions in its territory. One important …
allow a single definition for any of the given medical conditions in its territory. One important …
Erythrocyte microRNAs: a tiny magic bullet with great potential for sickle cell disease therapy
Sickle cell disease (SCD) is a severe hereditary blood disorder caused by a mutation of the
beta-globin gene, which results in a substantial reduction in life expectancy. Many studies …
beta-globin gene, which results in a substantial reduction in life expectancy. Many studies …
Ocular Presentations of Sickle Cell Disease Patients in a Nigerian Hospital
CC Efobi, OS Ejiofor, BC Ochiogu… - … of Advances in …, 2020 - archive.paparesearch.co.in
Introduction: Sickle Cell Disease (SCD) is an inherited haemolytic disorder that affects
virtually all body systems including the eye. Ocular complications of SCD could have dire …
virtually all body systems including the eye. Ocular complications of SCD could have dire …
[PDF][PDF] ACE I/D polymorphism is not a genetic modifier of renal features in sickle cell anemia patients
L Bhaskar, S Pattnaik - Journal of Renal Endocrinology, 2022 - pdfs.semanticscholar.org
Introduction: Sickle cell anemia (SCA) exhibits a host of complications that contribute to
increased morbidity and mortality at the youngest ages. Objectives: The aim of this …
increased morbidity and mortality at the youngest ages. Objectives: The aim of this …
High Systolic Blood Pressure, Anterior Segment Changes and Visual Impairment Independently Predict Sickle Cell Retinopathy
Sickle cell disease is often complicated by retinopathy, which can be proliferative or non
proliferative. Proliferative sickle cell retinopathy potentially leads to blindness. There is a …
proliferative. Proliferative sickle cell retinopathy potentially leads to blindness. There is a …
Genetic association of GSTM1, GSTT1, and GSTP1 polymorphisms with sickle cell disease complications: A systematic review and meta-analysis
Background Sickle cell disease (SCD) is a monogenic blood disorder characterized by vaso-
occlusive crises (VOC) also recurrent episodes of severe pain. Glutathione S-transferase …
occlusive crises (VOC) also recurrent episodes of severe pain. Glutathione S-transferase …
[PDF][PDF] A SYSTEMATIC REVIEW ON ABNORMAL HEMOGLOBIN OF SICKLE CELL DISORDER PATIENTS
S Das, BP Dash - researchgate.net
With a populace of over 1.2 billion people, it is anticipated that our country is domestic to
over fifty percent of the arena's SCD (Sickle Cell Disease) sufferers (Kate et. al., 2002) …
over fifty percent of the arena's SCD (Sickle Cell Disease) sufferers (Kate et. al., 2002) …
[HTML][HTML] Ocular Complications in Sickle Cell Disease: A Neglected Issue
H Al-Jafar, N Abul, Y Al-Herz, N Kumar - Open Journal of Ophthalmology, 2020 - scirp.org
Sickle cell disease is a common genetic blood disorder. It causes severe systemic
complications including ocular involvement. The degree of ocular complications is not …
complications including ocular involvement. The degree of ocular complications is not …
[PDF][PDF] Coinheritance of-3.7 Alpha-Thalassaemia Deletions Among Sickle Cell Anaemia Patients in Chhattisgarh, India
S Swarnakar, PK Patra, PK Khodiar… - Malaysian Journal of …, 2020 - researchgate.net
Abstract Background: Alpha (α)-thalassaemia is inherited as an autosomal recessive
disorder characterised by microcytic hypochromic anaemia. In children with homozygous …
disorder characterised by microcytic hypochromic anaemia. In children with homozygous …