thalassemia minor

thalassemia

[thal″ah-se´me-ah] a heterogeneous group of hereditary hemolytic anemias marked by a decreased rate of synthesis of one or more hemoglobin polypeptide chains, classified according to the chain involved (α, β, δ); the two major categories are α- and β-thalassemia.α-thalassemia (alpha-thalassemia) that caused by diminished synthesis of alpha chains of hemoglobin. The homozygous form is incompatible with life, the stillborn infant displaying severe hydrops fetalis. The heterozygous form may be asymptomatic or marked by mild anemia.β-thalassemia (beta-thalassemia) that caused by diminished synthesis of beta chains of hemoglobin. The homozygous form is called t. major and the heterozygous form is called t. minor.thalassemia ma´jor the homozygous form of β-thalassemia, in which hemoglobin A is completely absent; it appears in the newborn period and is marked by hemolytic, hypochromic, microcytic anemia; hepatosplenomegaly; skeletal deformation; mongoloid facies; and cardiac enlargement. thalassemia mi´nor the heterozygous form of β-thalassemia; it is usually asymptomatic, but there may be mild anemia.sickle cell–thalassemia a hereditary anemia involving simultaneous heterozygosity for hemoglobin S and thalassemia.

thal·as·se·mi·a mi·nor

[MIM*141800-142310 passim] the heterozygous state of a thalassemia gene or a hemoglobin Lepore gene; usually asymptomatic and quite variable hematologically, with target cells, mild hypochromic microcytosis, and often slightly reduced hemoglobin level with slightly increased erythrocyte count; types of hemoglobin are variable and depend on the gene involved.

thalassemia minor

Thalassemia trait Hematology The carrier state for beta thalassemia–heterozygosity, possession of one thalassemia gene; the person is essentially normal

thal·as·se·mi·a mi·nor

(thal'ă-sē'mē-ă mī'nŏr) The heterozygous state of a thalassemia gene or a hemoglobin Lepore gene; usually asymptomatic and widely variable hematologically, with target cells, mild hypochromic microcytosis, and often slightly reduced hemoglobin level with slightly increased erythrocyte count; types of hemoglobin are variable and depend on the gene involved.
Synonym(s): thalassaemia minor.

Cooley,

Thomas B., U.S. pediatrician, 1871-1945. Cooley anemia - the syndrome of severe anemia with multiple organ disorders. Synonym(s): thalassemia majorCooley trait - Synonym(s): thalassemia minor

thal·as·se·mi·a mi·nor

(thal'ă-sē'mē-ă mī'nŏr) [MIM*141800142310 passim, MIM*141800, MIM*141800-142310 passim] Heterozygous state of a thalassemia gene or a hemoglobin Lepore gene; usually asymptomatic and quite variable hematologically.
Synonym(s): thalassaemia minor.

单词	thalassemia minor
释义	DictionarySeethalassemiaEncyclopediaSeeThalassemia thalassemia minor thalassemia [thal″ah-se´me-ah] a heterogeneous group of hereditary hemolytic anemias marked by a decreased rate of synthesis of one or more hemoglobin polypeptide chains, classified according to the chain involved (α, β, δ); the two major categories are α- and β-thalassemia.α-thalassemia (alpha-thalassemia) that caused by diminished synthesis of alpha chains of hemoglobin. The homozygous form is incompatible with life, the stillborn infant displaying severe hydrops fetalis. The heterozygous form may be asymptomatic or marked by mild anemia.β-thalassemia (beta-thalassemia) that caused by diminished synthesis of beta chains of hemoglobin. The homozygous form is called t. major and the heterozygous form is called t. minor.thalassemia ma´jor the homozygous form of β-thalassemia, in which hemoglobin A is completely absent; it appears in the newborn period and is marked by hemolytic, hypochromic, microcytic anemia; hepatosplenomegaly; skeletal deformation; mongoloid facies; and cardiac enlargement. thalassemia mi´nor the heterozygous form of β-thalassemia; it is usually asymptomatic, but there may be mild anemia.sickle cell–thalassemia a hereditary anemia involving simultaneous heterozygosity for hemoglobin S and thalassemia. thal·as·se·mi·a mi·nor [MIM141800-142310 passim] the heterozygous state of a thalassemia gene or a hemoglobin Lepore gene; usually asymptomatic and quite variable hematologically, with target cells, mild hypochromic microcytosis, and often slightly reduced hemoglobin level with slightly increased erythrocyte count; types of hemoglobin are variable and depend on the gene involved. thalassemia minor Thalassemia trait Hematology The carrier state for beta thalassemia–heterozygosity, possession of one thalassemia gene; the person is essentially normal thal·as·se·mi·a mi·nor (thal'ă-sē'mē-ă mī'nŏr) The heterozygous state of a thalassemia gene or a hemoglobin Lepore gene; usually asymptomatic and widely variable hematologically, with target cells, mild hypochromic microcytosis, and often slightly reduced hemoglobin level with slightly increased erythrocyte count; types of hemoglobin are variable and depend on the gene involved. Synonym(s): thalassaemia minor. Cooley, Thomas B., U.S. pediatrician, 1871-1945. Cooley anemia* - the syndrome of severe anemia with multiple organ disorders. Synonym(s): thalassemia majorCooley trait - Synonym(s): thalassemia minor thal·as·se·mi·a mi·nor (thal'ă-sē'mē-ă mī'nŏr) [MIM141800142310 passim, MIM141800, MIM*141800-142310 passim] Heterozygous state of a thalassemia gene or a hemoglobin Lepore gene; usually asymptomatic and quite variable hematologically. Synonym(s): thalassaemia minor.
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