Hemoglobin Leiden [beta 6 or 7 (A3 or A4) Glu leads to O] in a Yugoslavian woman arisen by a new mutation.
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Adult↗
Biomedical subjects
I Ruzdić
Publications and source records attributed to I Ruzdić.
[Enzymes in the diagnosis and surgical treatment of arterial occlusive diseases].
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Alanine Transaminase↗
Hemoglobin Beograd (alpha2beta2 121 Glu leads to Val) interacting with beta-thalassemia.
Hematological and biochemical findings in a family with hemoglobin (Hb) Beograd interacting with beta-thalassemia are presented. Hb Beograd (alpha2beta2 121 Gul leads to Val) was found in 3 members. In two members it interacted with beta-thalassemia. These two double heterozygotes had anemia of intermediate severity and splenomegaly. Studies with 51Cr and 59Fe showed a shortened life span of red cells and ineffective erythropoiesis. The abnormal Hb amounted to 86-87%, and Hb F to 5-7%. No Hb A was present. One subject of the family was heterozygous for Hb Beograd. He showed normal clinical and hematological findings. The abnormal hemoglobin was 38%. Four members of the family were heterozygotes for beta-thalassemia. The interaction between beta-thalassemia and beta-chain variants is discussed.
Adult↗
G6PD deficiency in two autochthonous Croatian families.
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Adolescent↗
[Hemoglobinopathies].
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Hemoglobins, Abnormal↗