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Hb Youngstown [ß101(G3)Glu → Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemia.
Edward, Heather L; Pisani, Louis Almero Du; Rodriguez-Romero, Walter E; Chaves-Villalobos, Jorge; Garcia-Quesada, Jonielle; Harris, Neil S; Luo, Hong-Yuan; Steinberg, Martin H; Forget, Bernard G; Chui, David H K.
Afiliación
  • Edward HL; Departments of Medicine, and Pathology and Laboratory Medicine, Division of Hematology/Oncology, Boston University School of Medicine , Boston, Massachusetts , USA .
Hemoglobin ; 38(6): 381-4, 2014.
Article en En | MEDLINE | ID: mdl-25347256
ABSTRACT
Hb Youngstown is a rare hemoglobin (Hb) variant caused by substitution of glutamic acid with alanine at amino acid residue 101 of the ß-globin chain as a result of an A > C transversion on the ß-globin gene nucleotide sequences [ß101(G3)Glu → Ala; HBB c.305A > C]. We now report three patients from two different families, one from South Africa and the other from Costa Rica, who are heterozygous for this Hb variant. All three carriers had marked hemolysis, consistent with Hb Youngstown being a highly unstable variant. The substitution of glutamic acid, a large and negatively charged amino acid, with alanine, a small and non polar amino acid, in the interface of the α1- and ß2-globin subunits might interfere with the transition between the oxy- and deoxyHb, and lead to Hb instability and hemolytic anemia.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hemoglobinas Anormales / Mutación Missense / Anemia Hemolítica Congénita Tipo de estudio: Diagnostic_studies Límite: Adult / Child / Female / Humans Idioma: En Revista: Hemoglobin Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hemoglobinas Anormales / Mutación Missense / Anemia Hemolítica Congénita Tipo de estudio: Diagnostic_studies Límite: Adult / Child / Female / Humans Idioma: En Revista: Hemoglobin Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos