The Hemoglobin E Syndromes. I. Hemoglobin E in Eti-Turks
نویسندگان
چکیده
منابع مشابه
The hemoglobin E syndromes. I. Hemoglobin E in Eti-Turks.
With the technical assistance of Kaniil Tanrikulu H EMOGLOBIN E has been found with variable frequency among peopies of southeast Asia, such as the Thais,’ ’” the Burmese,2 the Malasians,3 the Indonesians,4 ”4’ the Bengalis,5#{176}’5” and Filipinos,6 and Vcddas of Ceylon.T37h Sporadic cases have been encountered in other countries.6’8 In 1955 an example of the hemoglobin E trait was discovered ...
متن کاملHemoglobin S in Eti-Turks and the Allewits in Lebanon.
I ‘ ‘ HAS been known for sonic tulle that the Eti-Turks pOSSCSS tile iligheSt incidence of sickling in the white race.’ Several previous papers have diScussed the characteristics of these people and have described the incidence of abnormal genes responsible for thalassemia and abnormal hemoglohins.25 It was also pointed out in some of these i tpers that tile Eti-Turks and the Allewits of Syria ...
متن کاملHemoglobin e syndromes.
Hemoglobin (Hb) E is one of the world's most common and important mutations. It results in a heterogeneous group of disorders whose phenotype range from asymptomatic to severe. Hb E trait and Hb EE are mild disorders. The combination of Hb E and Hb S (Hb SE) results in a sickle cell disease syndrome similar to sickle beta(+) thalassemia. It is important to distinguish Hb E disorders diagnostica...
متن کاملHemoglobin E syndromes in Pakistani population
BACKGROUND Hemoglobin E is an important hemoglobin variant with a worldwide distribution. A number of hemoglobinopathies have been reported from Pakistan. However a comprehensive description of hemoglobin E syndromes for the country was never made. This study aimed to describe various hemoglobin E disorders based on hematological parameters and chromatography. The sub-aim was to characterize he...
متن کاملThe hemoglobin E thalassemias.
Hemoglobin E (HbE) is an extremely common structural hemoglobin variant that occurs at high frequencies throughout many Asian countries. It is a β-hemoglobin variant, which is produced at a slightly reduced rate and hence has the phenotype of a mild form of β thalassemia. Its interactions with different forms of α thalassemia result in a wide variety of clinical disorders, whereas its coinherit...
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ژورنال
عنوان ژورنال: Blood
سال: 1960
ISSN: 0006-4971,1528-0020
DOI: 10.1182/blood.v15.5.606.606