A Case of Misdiagnosis Caused by the Coinheritance of Hb G-Siriraj [ß7(A4)GluâLys; <i>HBB</i>: c.22G>A] and Hb H Disease.

Guan, Zhi-Yang; Zhong, Ze-Yan; Xu, Zhi-Bang; Chen, Jian-Hong; Liu, Yan-Hui

A Case of Misdiagnosis Caused by the Coinheritance of Hb G-Siriraj [ß7(A4)GluâLys; HBB: c.22G>A] and Hb H Disease.

Guan, Zhi-Yang; Zhong, Ze-Yan; Xu, Zhi-Bang; Chen, Jian-Hong; Liu, Yan-Hui.

Afiliação

Guan ZY; The First Clinical Medical College, Guangdong Medical University, Zhanjiang, Guangdong, People's Republic of China.
Zhong ZY; Department of Medical Genetics and Prenatal Diagnosis, Huizhou First Maternal and Child Health Care Hospital, Huizhou, People's Republic of China.
Xu ZB; Department of Medical Genetics and Prenatal Diagnosis, Huizhou First Maternal and Child Health Care Hospital, Huizhou, People's Republic of China.
Chen JH; Department of Medical Genetics and Prenatal Diagnosis, Huizhou First Maternal and Child Health Care Hospital, Huizhou, People's Republic of China.
Liu YH; Department of Medical Genetics and Prenatal Diagnosis, Huizhou First Maternal and Child Health Care Hospital, Huizhou, People's Republic of China.

Hemoglobin ; 46(6): 338-340, 2022 Nov.

Article em En | MEDLINE | ID: mdl-36691989

Assuntos

Hemoglobinas Anormais; Talassemia alfa; Talassemia beta; Feminino; Humanos; Talassemia alfa/epidemiologia; Talassemia beta/genética; Hemoglobinas Anormais/genética; Erros de Diagnóstico; Povo Asiático; Heterozigoto; Mutação

Palavras-chave

Capillary electrophoresis (CE); Hb G-Siriraj; Hb H disease; interaction; misdiagnosis

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemoglobinas Anormais / Talassemia beta / Talassemia alfa Tipo de estudo: Clinical_trials / Diagnostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

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