A pediatric case of congenital neutropenia with SRP54 gene mutation in which monocytosis and gingival swelling were useful in differentiating from autoimmune neutropenia.

Manabe, Toshihiko; Taku, Keisuke; Hoshina, Takayuki; Higuchi, Naoko; Karakawa, Shuhei; Kusuhara, Koichi

Manabe, Toshihiko; Taku, Keisuke; Hoshina, Takayuki; Higuchi, Naoko; Karakawa, Shuhei; Kusuhara, Koichi.

Afiliação

Manabe T; Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan.
Taku K; Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan.
Hoshina T; Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan.
Higuchi N; Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan.
Karakawa S; Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Science, Hiroshima, Japan.
Kusuhara K; Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan.

Pediatr Blood Cancer ; 69(9): e29648, 2022 09.

Article em En | MEDLINE | ID: mdl-35253356

Assuntos

Neutropenia; Criança; Síndrome Congênita de Insuficiência da Medula Óssea; Humanos; Mutação; Neutropenia/congênito; Neutropenia/diagnóstico; Neutropenia/genética; Partícula de Reconhecimento de Sinal/genética

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neutropenia Tipo de estudo: Diagnostic_studies Limite: Child / Humans Idioma: En Revista: Pediatr Blood Cancer Ano de publicação: 2022 Tipo de documento: Article

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