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Recurrent pneumonia in three patients with MECP2 duplication syndrome with aspiration as the possible cause.
Sugitate, Ryo; Muramatsu, Kazuhiro; Ogata, Tomomi; Goto, Masahide; Hayashi, Shin; Sawaura, Noriko; Kawada-Nagashima, Masako; Matsui, Atsushi; Yamagata, Takanori.
Afiliación
  • Sugitate R; Department of Pediatrics, Japanese Red Cross Maebashi Hospital, Maebashi, Japan.
  • Muramatsu K; Department of Pediatrics, Jichi Medical University, Tochigi, Japan. Electronic address: kaz-mura@jichi.ac.jp.
  • Ogata T; Department of Pediatrics, Gunma University Graduate School of Medicine, Maebashi, Japan.
  • Goto M; Department of Pediatrics, Jichi Medical University, Tochigi, Japan.
  • Hayashi S; Department of Genetics, Institute for Developmental Research, Aichi Developmental Disability Center, Kasugai, Japan; Department of Molecular Cytogenesis, Medical Research Institute and Graduate School of Medical and Dental Science, Tokyo Medical and Dental University, Tokyo, Japan.
  • Sawaura N; Department of Pediatrics, Gunma University Graduate School of Medicine, Maebashi, Japan.
  • Kawada-Nagashima M; Department of Pediatrics, Jichi Medical University, Tochigi, Japan.
  • Matsui A; Department of Pediatrics, Japanese Red Cross Maebashi Hospital, Maebashi, Japan.
  • Yamagata T; Department of Pediatrics, Jichi Medical University, Tochigi, Japan.
Brain Dev ; 44(7): 486-491, 2022 Aug.
Article en En | MEDLINE | ID: mdl-35351320

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neumonía / Trastornos Respiratorios / Discapacidad Intelectual Ligada al Cromosoma X Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neumonía / Trastornos Respiratorios / Discapacidad Intelectual Ligada al Cromosoma X Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article