Spontaneous resolution of refractory cytopenia of childhood with monosomy 7 in an infant without an identifiable genetic cause.

Tsang, Michelle M C; Ha, Shau Yin; Chan, Nelson; So, Chi Chiu; Cheuk, Daniel K L; Chan, Godfrey C F

Tsang, Michelle M C; Ha, Shau Yin; Chan, Nelson; So, Chi Chiu; Cheuk, Daniel K L; Chan, Godfrey C F.

Afiliação

Tsang MMC; Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong SAR.
Ha SY; Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Children's Hospital, Hong Kong SAR.
Chan N; Department of Pathology, Hong Kong Children's Hospital, Hong Kong SAR.
So CC; Department of Pathology, Hong Kong Children's Hospital, Hong Kong SAR.
Cheuk DKL; Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Children's Hospital, Hong Kong SAR.
Chan GCF; Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Children's Hospital, Hong Kong SAR.

Pediatr Blood Cancer ; 69(10): e29654, 2022 10.

Article em En | MEDLINE | ID: mdl-35389555

Assuntos

Deleção Cromossômica; Síndromes Mielodisplásicas; Cromossomos Humanos Par 7/genética; Humanos; Lactente; Síndromes Mielodisplásicas/genética

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Deleção Cromossômica Idioma: En Ano de publicação: 2022 Tipo de documento: Article

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