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Ocular findings in a case of Pierson syndrome with a novel mutation in laminin ß2 gene.
Arima, Mitsuru; Tsukamoto, Shoko; Akiyama, Rumi; Nishiyama, Kei; Kohno, Ri-Ichiro; Tachibana, Takashi; Hayashida, Akira; Murayama, Miwa; Hisatomi, Toshio; Nozu, Kandai; Iijima, Kazumoto; Ohga, Shouichi; Sonoda, Koh-Hei.
Afiliación
  • Arima M; Department of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka City, Japan. Electronic address: m-arima@eye.med.kyushu-u.ac.jp.
  • Tsukamoto S; Department of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka City, Japan.
  • Akiyama R; Department of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka City, Japan.
  • Nishiyama K; Department of Pediatrics, Kyushu University Graduate School of Medical Sciences, Fukuoka City, Japan.
  • Kohno RI; Department of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka City, Japan.
  • Tachibana T; Department of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka City, Japan.
  • Hayashida A; Department of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka City, Japan.
  • Murayama M; Department of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka City, Japan.
  • Hisatomi T; Department of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka City, Japan.
  • Nozu K; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe City, Japan.
  • Iijima K; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe City, Japan.
  • Ohga S; Department of Pediatrics, Kyushu University Graduate School of Medical Sciences, Fukuoka City, Japan.
  • Sonoda KH; Department of Ophthalmology, Kyushu University Graduate School of Medical Sciences, Fukuoka City, Japan.
J AAPOS ; 22(5): 401-403.e1, 2018 Oct.
Article en En | MEDLINE | ID: mdl-30120985
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Degeneración Retiniana / Anomalías Múltiples / Catarata / Anomalías del Ojo / Trastornos de la Pupila / Laminina / Miopía Degenerativa / Mutación / Síndrome Nefrótico Tipo de estudio: Diagnostic_studies Límite: Humans / Infant / Male Idioma: En Revista: J AAPOS Asunto de la revista: OFTALMOLOGIA / PEDIATRIA Año: 2018 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
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XML
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Degeneración Retiniana / Anomalías Múltiples / Catarata / Anomalías del Ojo / Trastornos de la Pupila / Laminina / Miopía Degenerativa / Mutación / Síndrome Nefrótico Tipo de estudio: Diagnostic_studies Límite: Humans / Infant / Male Idioma: En Revista: J AAPOS Asunto de la revista: OFTALMOLOGIA / PEDIATRIA Año: 2018 Tipo del documento: Article Pais de publicación: Estados Unidos