A Case of EEC Syndrome with Pathypopituitary and Bilateral Hydronephrosis

DOI 20 References
  • INO Akira
    Department of Oral and Maxillo-Facial Surgery, Oita Medical University
  • FURUKAWA Masahide
    Department of Oral and Maxillo-Facial Surgery, Oita Medical University
  • MATSUMOTO Yushi
    Department of Oral and Maxillo-Facial Surgery, Oita Medical University
  • TAKAHASHI Yoshihiro
    Department of Oral and Maxillo-Facial Surgery, Oita Medical University
  • MIZUKI Harumi
    Department of Oral and Maxillo-Facial Surgery, Oita Medical University
  • YANAGISAWA Shigetaka
    Department of Oral and Maxillo-Facial Surgery, Oita Medical University

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Other Title
  • 汎下垂体機能低下症,両側水腎症を合併したEEC症候群の一例

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Description

EEC syndrome is characterized by ectrodactyly, ectodermal dysplasia, cleft lip and palate.<BR>Recently, a case of EEC syndrome accompanied with pathypopituitary, bilateral hydronephrosis and megalo ureter was encountered at our hospital.<BR>Deficiency of kidney function was observed for 1 month because of stenosis of the ureterovesical transmigration and inappropriate secretion of antidiuretic hormone. When bilateral cheiloplasty was performed, careful control of water and electrolyte was prepared. At the perioperation of palate plasty, there was no noticeable trouble. The operation was successful, and there were no complications.

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