The sickle cell (HbS) gene occurs at a variable frequency in the Middle Eastern Arab
countries, with characteristic distribution patterns and representing an overall picture of …

Haemoglobinopathies including the thalassemias and sickle cell disease are known to be
prevalent inherited disorders in most Arab countries with varying prevalence rates and …

Beta-thalassaemia major and sickle-cell disease are important health problems in Iraq. To
provide information for a prevention programme, the frequency of haemoglobin disorders …

The population in Jordan mounted from half a million in 1952 to 5.3 millions in 2004 and is
composed of a variety of ethnic groups, the majority being Arabs. Couples nowadays tend to …

Objectives: This investigation aimed to compare the radiographic changes and root and
crown-body lengths of the mandibular first permanent molar in a group of thalassaemic …

Thalassemia are inherited hematological disorders considered among the most common
genetic disorders worldwide, occurring more frequently in the Mediterranean Region. The …

Objective. The aim of this study was to examine the arch dimensions of Jordanian patients
with β‐thalassaemia major in comparison with an unaffected control group. Methods. The …

Dental development in subjects with thalassemia major. - Abstract - Europe PMC Sign in |
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Thalassemia is an inherited blood disorder that affects both genders and results in reduced
synthesis of hemoglobin, and thus causing anemia. Previous studies have shown that the …

Ethnopharmacological relevance Gundelia tournefortii is a member of the Asteraceae
(Compositae) family which is widely consumed as edible plant in the Eastern …