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The first case report of McLeod syndrome in a Chinese patient.
Man, B L; Yuen, Y P; Yip, S F; Ng, S H.
Afiliação
  • Man BL; Department of Medicine and Geriatrics, Tuen Mun Hospital, Hong Kong, Hong Kong. beli_man@yahoo.com
BMJ Case Rep ; 20132013 Aug 13.
Article em En | MEDLINE | ID: mdl-23943810
We report the first case of McLeod syndrome (MLS) in a 47-year-old Chinese man who presented with progressive limb weakness, chorea of feet, red blood cell acanthocytosis, absence of Kx red blood cell antigen and weak expression of Kell antigens. The diagnosis of MLS was confirmed by genetic testing showing a hemizygous mutation of XK gene. We review literature on neuroacanthocytosis in the Chinese population.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuroacantocitose Tipo de estudo: Diagnostic_studies Limite: Humans / Male / Middle aged Idioma: En Revista: BMJ Case Rep Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuroacantocitose Tipo de estudo: Diagnostic_studies Limite: Humans / Male / Middle aged Idioma: En Revista: BMJ Case Rep Ano de publicação: 2013 Tipo de documento: Article