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A Case Report of Scimitar Syndrome Associated with Pseudohermaphrodism Yasushi Kawaue 1 , Makoto Matsumura 1 , Nobukazu Miyoshi 1 , Takashi Kodama 1 , Kazumi Taguchi 1 , Akihiro Kishi 2 1The 1st Department of Surgery, Hiroshima University, School of Medicine 2Kake Hospital pp.415-418
Published Date 1980/4/15
DOI https://doi.org/10.11477/mf.1404203554
  • Abstract
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Scimitar syndrome is a rare congenital anomaly consisting of hypoplasia of the right lung, the right deviation of the heart, and anomalous pulmonary venous drainage to the inferior vena cava.

A case of 5 years old girl of Scimitar Syndrome associated with pseudohermaphrodism, was re-ported. The patient was operated upon with right pulmonary vein-left atrium anastomosis, and had a fair postoperative result.


Copyright © 1980, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1200 印刷版ISSN 0452-3458 医学書院

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