Sickle cell disease (SCD) is a major healthcare and societal problem affecting millions of people worldwide. In United States of America (USA), it is the most common genetic disorder affecting more than 80,000 people per year; majority of which are the African Americans Arabian and Indian. It is a genetic blood disorder affecting the red blood cells. Sickle cell pain is the hallmark of sickle cell disease and is associated with a very high mortality and morbidity rates. Being a genetic abnormality, the complete eradication of the disease from the affected seems to be difficult. Genetic counselling during pregnancy being the prime preventive step, Hematopoietic stem cell transplantation becomes the mainstay of treatment for complete eradicat...
Sickle cell disease (SCD) is an inherited red blood cell disorder caused by a structural abnormality...
Sickle cell disease (SCD) is an inherited red blood cell disorder caused by a structural abnormality...
Sickle cell disease is an autosomal recessive, multisystem disorder, characterised by chronic haemol...
Sickle cell disease is a group of disorders that affects hemoglobin, and causes distorted sickle- or...
Sickle cell disease (SCD) is a single gene disorder causing a debilitating systemic syndrome charact...
Sickle cell disease (SCD) is a collection of autosomal recessive genetic disorders involving the abn...
Sickle cell disease is a genetic disorder involving the haemoglobin designated as haemoglobin S, an ...
Sickle cell disease (SCD) is one of the most common genetic blood disorders in the world and affects...
Sickle cell disease (SCD) has no known genetic cure, although there have been recent significant str...
Sickle cell disease (SCD) is one of the most common genetic blood disorders in the world and affects...
Sickle cell disease (SCD) is the most common genetic disorder identified by newborn screening in the...
Sickle cell disease (SCD) is an inherited, lifelong condition. The sickle mutation consists a single...
Sickle cell disease (SCD) is usually caused due to the alteration of the beta-globin subunit in the ...
The purpose of this research timeline is to explore the history, prevalence, and effects of Sickle C...
Sickle cell disease (SCD) is a genetic condition that is present at birth. It is inherited when a ch...
Sickle cell disease (SCD) is an inherited red blood cell disorder caused by a structural abnormality...
Sickle cell disease (SCD) is an inherited red blood cell disorder caused by a structural abnormality...
Sickle cell disease is an autosomal recessive, multisystem disorder, characterised by chronic haemol...
Sickle cell disease is a group of disorders that affects hemoglobin, and causes distorted sickle- or...
Sickle cell disease (SCD) is a single gene disorder causing a debilitating systemic syndrome charact...
Sickle cell disease (SCD) is a collection of autosomal recessive genetic disorders involving the abn...
Sickle cell disease is a genetic disorder involving the haemoglobin designated as haemoglobin S, an ...
Sickle cell disease (SCD) is one of the most common genetic blood disorders in the world and affects...
Sickle cell disease (SCD) has no known genetic cure, although there have been recent significant str...
Sickle cell disease (SCD) is one of the most common genetic blood disorders in the world and affects...
Sickle cell disease (SCD) is the most common genetic disorder identified by newborn screening in the...
Sickle cell disease (SCD) is an inherited, lifelong condition. The sickle mutation consists a single...
Sickle cell disease (SCD) is usually caused due to the alteration of the beta-globin subunit in the ...
The purpose of this research timeline is to explore the history, prevalence, and effects of Sickle C...
Sickle cell disease (SCD) is a genetic condition that is present at birth. It is inherited when a ch...
Sickle cell disease (SCD) is an inherited red blood cell disorder caused by a structural abnormality...
Sickle cell disease (SCD) is an inherited red blood cell disorder caused by a structural abnormality...
Sickle cell disease is an autosomal recessive, multisystem disorder, characterised by chronic haemol...