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A case of 17q12 deletion syndrome that presented antenatally with markedly enlarged kidneys and clinically mimicked autosomal recessive polycystic kidney disease.
Nakamura, Misako; Kanda, Shoichiro; Kajiho, Yuko; Morisada, Naoya; Iijima, Kazumoto; Harita, Yutaka.
Afiliação
  • Nakamura M; Department of Pediatrics, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
  • Kanda S; Department of Pediatrics, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan. skanda-tky@umin.ac.jp.
  • Kajiho Y; Department of Pediatrics, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
  • Morisada N; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 650-0017, Japan.
  • Iijima K; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo, Kobe, Hyogo, 650-0017, Japan.
  • Harita Y; Department of Pediatrics, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
CEN Case Rep ; 10(4): 543-548, 2021 11.
Article em En | MEDLINE | ID: mdl-33942272
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 17 / Deleção Cromossômica / Rim Policístico Autossômico Recessivo Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 17 / Deleção Cromossômica / Rim Policístico Autossômico Recessivo Idioma: En Ano de publicação: 2021 Tipo de documento: Article