R1933X mutation in the MYH9 gene in May-Hegglin anomaly mimicking idiopathic thrombocytopenic purpura.

Sung, Chih-Chien; Lin, Shih-Hua; Chao, Tai-Kuang; Chen, Yeu-Chin

Sung, Chih-Chien; Lin, Shih-Hua; Chao, Tai-Kuang; Chen, Yeu-Chin.

Afiliação

Sung CC; Division of Nephrology, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Lin SH; Division of Nephrology, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Chao TK; Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Chen YC; Division of Hematology/Oncology, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan. Electronic address: yeu-chin@yahoo.com.tw.

J Formos Med Assoc ; 113(1): 56-9, 2014 Jan.

Article em En | MEDLINE | ID: mdl-23759689

Assuntos

Diagnóstico Diferencial; Proteínas Motores Moleculares/genética; Mutação; Cadeias Pesadas de Miosina/genética; Púrpura Trombocitopênica Idiopática/diagnóstico; Trombocitopenia/diagnóstico; Trombocitopenia/genética; Adulto; Humanos; Masculino

Palavras-chave

MYH9-related disorder; giant platelets; leukocyte inclusions

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trombocitopenia / Púrpura Trombocitopênica Idiopática / Cadeias Pesadas de Miosina / Proteínas Motores Moleculares / Diagnóstico Diferencial / Mutação Tipo de estudo: Diagnostic_studies Limite: Adult / Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article

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