Sindrome di Williams. Considerazioni su un caso insolito.

Translated title of the contribution: Williams syndrome. Considerations on an unusual case

M. G. Alpigiani, G. Franzone, M. G. Puleo, A. Carpi, A. Iester

Research output: Contribution to journalArticle

Abstract

We report one case of WS, who came at our first observation at age of eight for mental retardation and congenial cardiopathy of unknown origin. Echocardiography and Doppler examination showed immediately isthmic aortic stenosis, and therefore aortic plastic surgery was performed, with a good post-operative result. The case aroused the interest of the Authors, owing to the late diagnosis of aortic coarctation, which, however, did not produce hemodynamic alteration.

Translated title of the contributionWilliams syndrome. Considerations on an unusual case
Original languageItalian
Pages (from-to)85-86
Number of pages2
JournalPediatria Medica e Chirurgica
Volume16
Issue number1
Publication statusPublished - Jan 1994

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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  • Cite this

    Alpigiani, M. G., Franzone, G., Puleo, M. G., Carpi, A., & Iester, A. (1994). Sindrome di Williams. Considerazioni su un caso insolito. Pediatria Medica e Chirurgica, 16(1), 85-86.