Treatment of sickle cell disease remains largely palliative. While it may improve the quality of life, persons with sickle cell disease still suffer from extreme sickling crises, end-organ damage, and reduced life expectancy. Increasing studies have led to the identification and advancement of stem cell transplant and gene therapy as potential curative strategies for sickle cell disease. However, there have been various factors that have hindered their clinical application. Stem cell transplantation, the more propitious of the two, is limited by restricted transplant donor pool, transplant complications, and selection criteria. The current paper reviewed the literature on sickle cell disease, current treatment options, and more particularly...
Thalassemia major and sickle cell disease are the two most widely disseminated hereditary hemoglobin...
which permits unrestricted use, distribution, and reproduction in any medium, provided the original ...
Sickle cell disease and its variants constitute the most common inherited blood disorders affecting ...
Background: Sickle cell anemia (SCA) is an inherited monogenic disorder. The clinical symptoms of SC...
Sickle cell disease is a genetic disorder caused by sickle haemoglobin. In many forms of the disease...
Allogeneic HSCT controls sickle cell disease (SCD)–related organ damage and is currently the only cu...
Over 70,000 people live with sickle cell disease (SCD) in the United States and multitudes worldwide...
Sickle cell disease (SCD) is an inherited disorder of hemoglobin structure that has no established c...
Sickle cell disease is an autosomal recessive, multisystem disorder, characterised by chronic haemol...
Sickle cell disease (SCD; ORPHA232; OMIM # 603903) is a chronic and invalidating disorder distribute...
The objective of hematopoietic cell transplantation (HCT), and of replacement gene therapy for sickl...
The sickle hemoglobin is an abnormal hemoglobin due to point mutation (GAG → GTG) in exon 1 of the β...
Monica Bhatia,1 Sujit Sheth21Division of Pediatric Hematology/Oncology/Stem Cell Transplantation, Co...
Hematopoietic stem cell transplant (HSCT) is the only readily available curative option for sickle c...
Sickle cell disease (SCD) has no known genetic cure, although there have been recent significant str...
Thalassemia major and sickle cell disease are the two most widely disseminated hereditary hemoglobin...
which permits unrestricted use, distribution, and reproduction in any medium, provided the original ...
Sickle cell disease and its variants constitute the most common inherited blood disorders affecting ...
Background: Sickle cell anemia (SCA) is an inherited monogenic disorder. The clinical symptoms of SC...
Sickle cell disease is a genetic disorder caused by sickle haemoglobin. In many forms of the disease...
Allogeneic HSCT controls sickle cell disease (SCD)–related organ damage and is currently the only cu...
Over 70,000 people live with sickle cell disease (SCD) in the United States and multitudes worldwide...
Sickle cell disease (SCD) is an inherited disorder of hemoglobin structure that has no established c...
Sickle cell disease is an autosomal recessive, multisystem disorder, characterised by chronic haemol...
Sickle cell disease (SCD; ORPHA232; OMIM # 603903) is a chronic and invalidating disorder distribute...
The objective of hematopoietic cell transplantation (HCT), and of replacement gene therapy for sickl...
The sickle hemoglobin is an abnormal hemoglobin due to point mutation (GAG → GTG) in exon 1 of the β...
Monica Bhatia,1 Sujit Sheth21Division of Pediatric Hematology/Oncology/Stem Cell Transplantation, Co...
Hematopoietic stem cell transplant (HSCT) is the only readily available curative option for sickle c...
Sickle cell disease (SCD) has no known genetic cure, although there have been recent significant str...
Thalassemia major and sickle cell disease are the two most widely disseminated hereditary hemoglobin...
which permits unrestricted use, distribution, and reproduction in any medium, provided the original ...
Sickle cell disease and its variants constitute the most common inherited blood disorders affecting ...