Thalassemia and Sickle Cell Disease (SCD) both are genetic blood disorders occurring by destruction in red blood cells (RBCs). Every year about 300,000 infants worldwide are born with Thalassemia syndrome (30 per cents) and sickle cell anaemia (70 per cents. Globally, the percentage of carriers of Thalassemia is greater than that of carriers of SCA, but because of the high frequency of the sick...

BACKGROUND & AIM it is well known that hydroxyurea impacts on clinical and hematologic indices in sickle cell disease (SCD), we aimed to evaluate the effect of hydroxyurea on clinical and hematological improvement of sickle cell anemia. METHODS & MATERIALS In this cohort study 48 patients with sickle cell disease were enrolled and pain crisis, severity of pain, acute chest syndrome, the numbe...

Physicians have long been intrigued by the unusual cardiac and pulmonary manifestations which may occur in patients with sickle cell anemia. Cardiomegaly, systolic and diastolic murmurs, recurrent bouts of pulmonary infiltration and chest pain, episodic or chronic dyspnea all of these may appear in the sicklemic individual. In recent years, considerable investigation has been carried out to def...

Supporting cells (SCs) of the cochlear (auditory) and vestibular (balance) organs hold promise as a platform for therapeutic regeneration of the sensory hair cells. Prior data have shown proliferative restrictions of adult SCs forced to re-enter the cell cycle. By comparing juvenile and adult SCs in explant cultures, we have here studied how proliferative restrictions are linked with DNA damage...

The objective of this study was to analyze the association of somatic cell score (SCS) with milk, fat and protein yields across parities. Records of production traits and somatic cell counts (SCC) from first, second and third parity that were collected by the Animal Breeding Center of Iran from 1993 to 2010 were used.All animals were grouped into six classes according to SCC and production trai...

A Ghanaian family is described in which a sickle-cell haemoglobin C man married to a sickle-cell thalassaemia woman produced 12 children (eight alive). Four children have sickle-cell anaemia, two sickle-cell haemoglobin C disease, one has sickle-cell thalassaemia, and one is asymptomatic haemoglobin C thalassaemia.It is emphasized that the contribution that adult sickle-cell disease patients ma...