Sickle cell disease (SCD) is a group of blood disorders typically inherited from a person's
parents. The most common type is known as sickle cell anemia (SCA), is hemoglobin …

Objectives: To determine the D-dimer levels and some hematological parameters of adult
patients with sickle cell anemia in steady state attending the hematology clinic of Ahmadu …

Aim: This study aimed to assess the D-dimer levels and platelet count in sickle cell anaemia
patients and compare with those of the control subjects. Materials and Methods: This study is …

Background: Sickle cell anemia (SCA) has been linked with altered plasma levels of D‑
dimer. However, routine assessment of D‑dimer and other coagulation indices in SCA …

Introduction: A sickle cell anaemia one of a haemoglobinopathy, which constituted as a
model for genetically inherited disorders, the course of the disease involves may crises, the …

BACKGROUND Sickle cell anaemia (SCD) is a global genetic disease. Potential changes in
multiple biochemical indices are also often a major factor behind the varied clinical …

Background: Sickle cell disease (SCD) is an autosomal recessive disease caused by a
single gene mutation, leading to sickle-shaped red blood cells, causing many clinical …

Hydroxyurea (HU) is used as a disease-modifying agent in sickle cell disease (SCD). Its
beneficial effects have been ascribed to inhibition of the sickling process through increase of …

In this study, we examined the hematological parameters between sickle cell disease, sickle
cell trait and control individuals. Haematological parameters were compare among SS, AS …

Background: Sickle cell disease hemoglobinopathy gets inherited in autosomal recessive
pattern. In sickle cell disease substitution of amino acid valine for glutamic acid at the sixth …