Neuropediatrics 2008; 39(6): 335-340
DOI: 10.1055/s-0029-1216354
Original Article

© Georg Thieme Verlag KG Stuttgart · New York

Visual Function in Noonan and LEOPARD Syndrome

P. Alfieri 1 , 6 , L. Cesarini 1 , G. Zampino 2 , F. Pantaleoni 3 , A. Selicorni 4 , A. Salerni 5 , I. Vasta 2 , M. Cerutti 4 , A. Dickmann 5 , F. Colitto 1 , S. Staccioli 1 , C. Leoni 2 , D. Ricci 1 , C. Brogna 1 , M. Tartaglia 3 , E. Mercuri 1
  • 1Pediatric Neurology Unit, Catholic University, Rome, Italy
  • 2Servizio di Epidemiologia e Clinica dei Difetti Congeniti Istituto di Clinica Pediatrica, Catholic University, Rome, Italy
  • 3Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanità, Rome, Italy
  • 4Ambulatorio di Genetica clinica, I Clinica Pediatrica IRCCS Fondazione Policlinico Mangiagalli, Regina Elena, Milan, Italy
  • 5Department of Ophthalmology, Catholic University, Rome, Italy
  • 6IRCSS, Children's Hospital Bambinolesú, Rome, Italy
Further Information

Publication History

received 02.10.2008

accepted 02.03.2009

Publication Date:
30 June 2009 (online)

Abstract

The aim of the study was to assess various aspects of visual and visuoperceptual function in patients with Noonan syndrome (NS) or LEOPARD syndrome (LS) with mutations affecting the PTPN11, SOS1 and RAF1 genes. Twenty-four patients were assessed with a battery of tests assessing visual function including ophthalmological and orthoptic evaluation and age appropriate behavioural visual tests, including measures of crowding acuity (Cambridge crowding cards), and stereopsis (TNO test). Twenty-one subjects were also assessed with the visuo-motor integration (VMI) test. Twenty of the 24 patients (83%) had abnormalities of visual function on at least one of the tests used to assess visual function or on ophthalmological examination, and 7 of 21 (33%) also had abnormalities on VMI. Ocular movements and stereopsis were most frequently abnormal (50% and 79%, respectively). Our results suggest that visual and visuoperceptual abilities are commonly impaired in patients with Noonan and LEOPARD syndrome and they are probably related to a multifactorial etiology.

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Correspondence

Prof. E. Mercuri

Neuropsichiatria Infantile

Policlinico Gemelli

Largo Gemelli 8

00168 Rome

Italy

Phone: +39/06/3015 43 40

Fax: +39/06/3015 43 40

Email: mercuri@rm.unicatt.it

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