Visual Function in Noonan and LEOPARD Syndrome

被引:20
|
作者
Alfieri, P. [1 ,6 ]
Cesarini, L. [1 ]
Zampino, G. [2 ]
Pantaleoni, F. [3 ]
Selicorni, A. [4 ]
Salerni, A. [5 ]
Vasta, I. [2 ]
Cerutti, M. [4 ]
Dickmann, A. [5 ]
Colitto, F. [1 ]
Staccioli, S. [1 ]
Leoni, C. [2 ]
Ricci, D. [1 ]
Brogna, C. [1 ]
Tartaglia, M. [3 ]
Mercuri, E. [1 ]
机构
[1] Catholic Univ, Pediat Neurol Unit, Rome, Italy
[2] Catholic Univ, Serv Epidemiol & Clin Difetti Congeniti, Ist Clin Pediat, Rome, Italy
[3] Ist Super Sanita, Dipartimento Biol Cellulare & Neurosci, I-00161 Rome, Italy
[4] Policlin Mangiagalli, Clin Pediat IRCCS Fdn 1, Ambulatorio Genet Clin, Milan, Italy
[5] Catholic Univ, Dept Ophthalmol, Rome, Italy
[6] Childrens Hosp Bambinolesu, IRCSS, Rome, Italy
关键词
vision; Noonan syndrome; LEOPARD syndrome; genotype-phenotype;
D O I
10.1055/s-0029-1216354
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:335 / 340
页数:6
相关论文
共 50 条
  • [41] Noonan syndrome
    Yanagisawa, M
    ACTA PAEDIATRICA JAPONICA, 1996, 38 (01): : 75 - 75
  • [42] Noonan syndrome
    Turner, Anne M.
    JOURNAL OF PAEDIATRICS AND CHILD HEALTH, 2014, 50 (10) : E14 - E20
  • [43] Noonan syndrome
    Ineke van der Burgt
    Orphanet Journal of Rare Diseases, 2
  • [44] NOONAN SYNDROME
    LIN, AE
    JOURNAL OF MEDICAL GENETICS, 1988, 25 (01) : 64 - 65
  • [45] HYPOTHALAMO-HYPOPHYSEAL FUNCTION IN 2 PATIENTS WITH NOONAN SYNDROME
    SOSA, J
    BOLANOS, F
    MORATO, T
    REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION, 1978, 30 (02): : 219 - 220
  • [46] Impaired Sertoli Cell Function in Males Diagnosed with Noonan Syndrome
    Marcus, K. A.
    Sweep, C. G. J.
    van der Burgt, I.
    Noordam, C.
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2008, 21 (11): : 1079 - 1084
  • [47] The role of PTPN11 mutations in Noonan and LEOPARD syndromes
    Short, J
    Shaw, A
    Kalidas, K
    Jeffery, S
    Patton, M
    Taylor, R
    JOURNAL OF MEDICAL GENETICS, 2005, 42 : S99 - S99
  • [48] Phosphoproteomics-Mediated Identification of Fer Kinase as a Target of Mutant Shp2 in Noonan and LEOPARD Syndrome
    Overman, Jeroen Paardekooper
    Preisinger, Christian
    Prummel, Karin
    Bonetti, Monica
    Giansanti, Piero
    Heck, Albert
    den Hertog, Jeroen
    PLOS ONE, 2014, 9 (09):
  • [49] LEOPARD SYNDROME
    LYNCH, PJ
    ARCHIVES OF DERMATOLOGY, 1970, 101 (01) : 119 - &
  • [50] Leopard syndrome
    Sarkozy, Anna
    Digilio, Maria Cristina
    Dallapiccola, Bruno
    ORPHANET JOURNAL OF RARE DISEASES, 2008, 3 (1)