Literature DB >> 8745391

Neurologic findings in children and adults with Williams syndrome.

C A Chapman1, A du Plessis, B R Pober.   

Abstract

Twenty-four children with Williams syndrome underwent systematic neurologic evaluations. Abnormalities of mental status, motor coordination, tone, and gait were most prevalent. Tone abnormalities varied as a function of age, with younger children frequently exhibiting decreased tone and older subjects almost exclusively having increased tone. The gait and coordination abnormalities persisted among older subjects, indicating that they were not simply maturational problems. Physicians caring for such youngsters need to be aware that a variety of neurologic abnormalities are common in Williams syndrome and may change or progress over time. Neurologic examinations that reveal findings beyond the typical pattern that we report may raise suspicion for added neurologic insult and warrant further investigation.

Entities:  

Mesh:

Year:  1996        PMID: 8745391     DOI: 10.1177/088307389601100116

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  15 in total

1.  Visual depth processing in Williams-Beuren syndrome.

Authors:  J N Van der Geest; G C Lagers-van Haselen; J M van Hagen; E Brenner; L C P Govaerts; I F M de Coo; M A Frens
Journal:  Exp Brain Res       Date:  2005-06-18       Impact factor: 1.972

2.  Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome.

Authors:  Stefano Marenco; Michael A Siuta; J Shane Kippenhan; Samuel Grodofsky; Wei-Li Chang; Philip Kohn; Carolyn B Mervis; Colleen A Morris; Daniel R Weinberger; Andreas Meyer-Lindenberg; Carlo Pierpaoli; Karen Faith Berman
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-07       Impact factor: 11.205

Review 3.  Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.

Authors:  Daniel Paul Eisenberg; Mbemba Jabbi; Karen Faith Berman
Journal:  Neuroimage       Date:  2010-03-03       Impact factor: 6.556

Review 4.  Copy number variants at Williams-Beuren syndrome 7q11.23 region.

Authors:  Giuseppe Merla; Nicola Brunetti-Pierri; Lucia Micale; Carmela Fusco
Journal:  Hum Genet       Date:  2010-05-01       Impact factor: 4.132

5.  Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome.

Authors:  Andreas Meyer-Lindenberg; Carolyn B Mervis; Deepak Sarpal; Paul Koch; Sonya Steele; Philip Kohn; Stefano Marenco; Colleen A Morris; Saumitra Das; Shane Kippenhan; Venkata S Mattay; Daniel R Weinberger; Karen Faith Berman
Journal:  J Clin Invest       Date:  2005-06-09       Impact factor: 14.808

6.  Unpredictable postoperative global cerebral infarction in the patient of williams syndrome accompanying moyamoya disease.

Authors:  Yang-Won Sim; Mou-Seop Lee; Young-Gyu Kim; Dong-Ho Kim
Journal:  J Korean Neurosurg Soc       Date:  2011-09-30

7.  Alterations in diffusion properties of white matter in Williams syndrome.

Authors:  Lori R Arlinghaus; Tricia A Thornton-Wells; Elisabeth M Dykens; Adam W Anderson
Journal:  Magn Reson Imaging       Date:  2011-09-09       Impact factor: 2.546

8.  Abnormalities in neural processing of emotional stimuli in Williams syndrome vary according to social vs. non-social content.

Authors:  Karen E Muñoz; Andreas Meyer-Lindenberg; Ahmad R Hariri; Carolyn B Mervis; Venkata S Mattay; Colleen A Morris; Karen Faith Berman
Journal:  Neuroimage       Date:  2009-12-11       Impact factor: 6.556

9.  Sudden unexpected death in a toddler with Williams syndrome.

Authors:  Henry F Krous; Carter Wahl; Amy E Chadwick
Journal:  Forensic Sci Med Pathol       Date:  2008-04-04       Impact factor: 2.007

10.  Gait function in adults with Williams syndrome.

Authors:  Darren R Hocking; Nicole J Rinehart; Jennifer L McGinley; John L Bradshaw
Journal:  Exp Brain Res       Date:  2008-10-08       Impact factor: 1.972

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.