Unstable hemoglobin disorders are characterized by a congenital, mostly familial chronic hemolytic anemia with episodes of severe hemolysis during febrile illnesses. Usually, isopropanol and heat stability tests lead to the diagnosis which is confirmed by protein and gene sequencing. Generation of the mutations is still a subject of controversy. PATIENT, MATERIALS AND METHODS: We describe a 6-year-old Swiss child with congenital hemolytic anemia and a negative family history. Hemoglobin was studied by IEF, HPLC reverse phase chromatography, heat stability and isopropranol tests. DNA was sequenced in both coding and non-coding strands
A new unstable hemoglobin (Hb) variant, named Hb Aalesund, was detected during Hb A1c measurement in...
Fetal hemoglobin (Hb F) is characteristic of the fetal development period. However, in some genetic ...
Summary The haemoglobinopathies refer to a diverse group of inherited disorders characterized by a r...
Hemoglobins M and unstable hemoglobins cause clinical syndromes that are transmitted in autosomal do...
Three independent cases of chronic haemolytic anaemia in Sweden have recently been demonstrated to b...
We describe here two new unstable β-globin variants, Hb Caruaru and Hb Olinda, found in northeastern...
A 4-year-old boy, a β-thalassemia (β-thal) carrier, with an unexplained severe chronic microcytic an...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Ci...
A family was studied in which two inherited defects of the non-alpha-globin cluster segregate: Greek...
Unstable hemoglobinopathies (UHs) are rare anemia disorders (RADs) characterized by abnormal hemoglo...
International audienceHb Dompierre [β29(B11)Gly→Arg, HBB: c.88G>C] is a rare β-globin gene variant t...
Hemoglobin Hammersmith is a rare unstable variant of hemoglobin with decreased oxygen affinity. We r...
AbstractA new β-variant has been detected and structurally defined in a French male, with a life-lon...
Abstract A 20-year-old man has been under observation for 18 years because of unstable hemoglobinemi...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
A new unstable hemoglobin (Hb) variant, named Hb Aalesund, was detected during Hb A1c measurement in...
Fetal hemoglobin (Hb F) is characteristic of the fetal development period. However, in some genetic ...
Summary The haemoglobinopathies refer to a diverse group of inherited disorders characterized by a r...
Hemoglobins M and unstable hemoglobins cause clinical syndromes that are transmitted in autosomal do...
Three independent cases of chronic haemolytic anaemia in Sweden have recently been demonstrated to b...
We describe here two new unstable β-globin variants, Hb Caruaru and Hb Olinda, found in northeastern...
A 4-year-old boy, a β-thalassemia (β-thal) carrier, with an unexplained severe chronic microcytic an...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Ci...
A family was studied in which two inherited defects of the non-alpha-globin cluster segregate: Greek...
Unstable hemoglobinopathies (UHs) are rare anemia disorders (RADs) characterized by abnormal hemoglo...
International audienceHb Dompierre [β29(B11)Gly→Arg, HBB: c.88G>C] is a rare β-globin gene variant t...
Hemoglobin Hammersmith is a rare unstable variant of hemoglobin with decreased oxygen affinity. We r...
AbstractA new β-variant has been detected and structurally defined in a French male, with a life-lon...
Abstract A 20-year-old man has been under observation for 18 years because of unstable hemoglobinemi...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
A new unstable hemoglobin (Hb) variant, named Hb Aalesund, was detected during Hb A1c measurement in...
Fetal hemoglobin (Hb F) is characteristic of the fetal development period. However, in some genetic ...
Summary The haemoglobinopathies refer to a diverse group of inherited disorders characterized by a r...