Sindrome di Williams. Considerazioni su un caso insolito.

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

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

Istituto "Giannina Gaslini"

Research output: Contribution to journal › Article › peer-review

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 contribution	Williams syndrome. Considerations on an unusual case
Original language	Italian
Pages (from-to)	85-86
Number of pages	2
Journal	Pediatria Medica e Chirurgica
Volume	16
Issue number	1
Publication status	Published - Jan 1994

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health

Cite this

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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.",

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AU - Franzone, G.

AU - Puleo, M. G.

AU - Carpi, A.

AU - Iester, A.

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N2 - 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.

AB - 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.

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Sindrome di Williams. Considerazioni su un caso insolito.

Abstract

ASJC Scopus subject areas

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