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

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

Access to Document

Fingerprint Dive into the research topics of 'Williams syndrome. Considerations on an unusual case'. Together they form a unique fingerprint.

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.

@article{5835c918066f4f47a22307008b2b9f6a,

title = "Sindrome di Williams. Considerazioni su un caso insolito.",

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.",

author = "Alpigiani, {M. G.} and G. Franzone and Puleo, {M. G.} and A. Carpi and A. Iester",

year = "1994",

month = jan,

language = "Italian",

volume = "16",

pages = "85--86",

journal = "Pediatria Medica e Chirurgica",

issn = "0391-5387",

publisher = "Vicenza Pediatria Medica E Chirurgica",

number = "1",

}

TY - JOUR

T1 - Sindrome di Williams. Considerazioni su un caso insolito.

AU - Alpigiani, M. G.

AU - Franzone, G.

AU - Puleo, M. G.

AU - Carpi, A.

AU - Iester, A.

PY - 1994/1

Y1 - 1994/1

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.

UR - http://www.scopus.com/inward/record.url?scp=0028186935&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0028186935&partnerID=8YFLogxK

M3 - Articolo

C2 - 8029098

AN - SCOPUS:0028186935

VL - 16

SP - 85

EP - 86

JO - Pediatria Medica e Chirurgica

JF - Pediatria Medica e Chirurgica

SN - 0391-5387

IS - 1

ER -