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A CASE OF THE PRADER-WILLI SYNDROME Shuji Tokunaga 1 , Kazuo Murayama 1 1Department of Urology, School of Medicine, Kanazawa University pp.673-676
Published Date 1982/7/20
DOI https://doi.org/10.11477/mf.1413203394
  • Abstract
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The patient was a 5-year old boy by a full-term normal spontaneous delivery, weighing 2.7kg. The mother had realized an inertia of quickening of the fetus in utero during her pregnancy.

At a newborn infancy and early infancy, he was less active in body movement, cried weakly and was unable to swallow and suck sufficietly. In a later infancy, he had a mental retardation and limited vocabulary.

He was consulted by a doctor because of a loss of bilateral scrotal contents, at the age of 2, and diagnosed as bilateral cryptorchidism and hypoplasia of the penis and scrotum.


Copyright © 1982, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1332 印刷版ISSN 0385-2393 医学書院

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