Add to ORKGOnly five Hb S heterozygotes with an associated Hb H Disease i.e. the ASH condition or AS: --/-α have been defined in molecular detail. These had ancestries of Saudi-Arabian, Black or mixed Black and Chinese origin. We have studied a sixth patient who was from Turkey. The propositus was detected at birth with Hb Bart's at 27.6%. This declined to 1.6% at nine months, while the proportion of Hb S which was 5.1% at one month increased to 18.0% at one year.peer-reviewe
Sickle cell disease (SCD), caused by a mutation in the β-globin gene HBB, is widely distributed in m...
Sickle cell syndrome HbS/β thalassemia is an inheritable mendelian type disease where two affected a...
The distribution of clinical features was examined in subjects with homozygous sickle cell (SS) dise...
Sickle cell anemia is one of the first diseases to be understood at the molecular level. The amino a...
Studying different sickle cell genotypes may throw light on the pathogenesis of sickle cell disease ...
Sickle cell disease (SCD) is one of the commonest severe inherited disorders, but specific treatment...
S ICKLE CELL-THALASSEMIA DISEASE is known to be a severe or moderately severe type of congenital hem...
Sickle cell diseases comprise a group of genetic disorders characterized by the presence of hemoglob...
Sickle cell disease is the presence of two hemoglobin S alleles and results in sickle shaped red blo...
We present a case of a 40-year-old female from Turkey, who was referred to our outpatient clinic for...
Background: The term "sickle cell disease" refers to a collection of autosomal recessive genetic dis...
Sickle cell disease (SCD) is one of the commonest severe inherited disorders, but specific treatment...
Background: Sickle cell disease (SCD) and its variants are genetic disorders resulting from the pres...
Sickle Cell disease is a generic term for a group of genetic disorders characterized by the predomin...
Precision scale models of sickle cell hemoglobin molecules indicate that the genetic substitution of...
Sickle cell disease (SCD), caused by a mutation in the β-globin gene HBB, is widely distributed in m...
Sickle cell syndrome HbS/β thalassemia is an inheritable mendelian type disease where two affected a...
The distribution of clinical features was examined in subjects with homozygous sickle cell (SS) dise...
Sickle cell anemia is one of the first diseases to be understood at the molecular level. The amino a...
Studying different sickle cell genotypes may throw light on the pathogenesis of sickle cell disease ...
Sickle cell disease (SCD) is one of the commonest severe inherited disorders, but specific treatment...
S ICKLE CELL-THALASSEMIA DISEASE is known to be a severe or moderately severe type of congenital hem...
Sickle cell diseases comprise a group of genetic disorders characterized by the presence of hemoglob...
Sickle cell disease is the presence of two hemoglobin S alleles and results in sickle shaped red blo...
We present a case of a 40-year-old female from Turkey, who was referred to our outpatient clinic for...
Background: The term "sickle cell disease" refers to a collection of autosomal recessive genetic dis...
Sickle cell disease (SCD) is one of the commonest severe inherited disorders, but specific treatment...
Background: Sickle cell disease (SCD) and its variants are genetic disorders resulting from the pres...
Sickle Cell disease is a generic term for a group of genetic disorders characterized by the predomin...
Precision scale models of sickle cell hemoglobin molecules indicate that the genetic substitution of...
Sickle cell disease (SCD), caused by a mutation in the β-globin gene HBB, is widely distributed in m...
Sickle cell syndrome HbS/β thalassemia is an inheritable mendelian type disease where two affected a...
The distribution of clinical features was examined in subjects with homozygous sickle cell (SS) dise...