Literature DB >> 12223034

Williams syndrome: neuronal size and neuronal-packing density in primary visual cortex.

Albert M Galaburda1, Dorothy P Holinger, Ursula Bellugi, Gordon F Sherman.   

Abstract

BACKGROUND: Williams syndrome (WMS) is a rare, genetically based syndrome associated with a hemideletion in chromosome 7 (7q11.22-23) and characterized by a unique constellation of somatic, brain, and cognitive features. Individuals with WMS demonstrate an unusual and uneven neuropsychological profile showing cognitive and visual spatial deficits juxtaposed with relative language preservation and excellent facial recognition.
OBJECTIVES: A neuroanatomical hypothesis for these behavioral findings suggests predominant involvement of the dorsal portions of the hemispheres relative to the ventral portions, including preferential involvement of peripheral visual field cortical representations over central representation. Predominant involvement of magnocellular visual pathways, as opposed to parvocellular pathways, is also suggested by this hypothesis.
SUBJECTS: We examined primary visual cortical area 17 in the right and left hemispheres in 6 age- and sex-matched autopsy specimens from 3 WMS-affected brains (1 male and 2 females; mean [SD] age, 44 [14] years) and 3 control brains (1 male and 2 females; mean age, 43 [11] years).
DESIGN: Neurons in layers II, III, IVA, IVB, IVCalpha, IVCbeta, V, and VI were measured using an optical dissector method to determine possible differences between WMS-affected and control brains in cell-packing density, neuronal size, and neuronal size distribution.
RESULTS: We found abnormalities in peripheral visual cortex in WMS-affected brains, but not in magnocellular subdivisions. There was a hemisphere by layer IV interaction and a layer IV left hemisphere and diagnosis interaction in cell-packing density. Williams syndrome-affected brains showed increased cell-packing density in left sublayer IVCbeta and an excess of small neurons in left layers IVA, IVCalpha, IVCbeta, V, and VI.
CONCLUSIONS: Cell measurements differ in peripheral visual cortical fields of WMS, with significantly smaller, more closely packed cells in some layers on the left side. These cell-packing density and neuronal size differences may be related to visuospatial deficits in this population.

Entities:  

Mesh:

Year:  2002        PMID: 12223034     DOI: 10.1001/archneur.59.9.1461

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  25 in total

1.  Callosal morphology in Williams syndrome: a new evaluation of shape and thickness.

Authors:  Eileen Luders; Margherita Di Paola; Francesco Tomaiuolo; Paul M Thompson; Arthur W Toga; Stefano Vicari; Michael Petrides; Carlo Caltagirone
Journal:  Neuroreport       Date:  2007-02-12       Impact factor: 1.837

2.  Retinotopically defined primary visual cortex in Williams syndrome.

Authors:  Rosanna K Olsen; J Shane Kippenhan; Shruti Japee; Philip Kohn; Carolyn B Mervis; Ziad S Saad; Colleen A Morris; Andreas Meyer-Lindenberg; Karen Faith Berman
Journal:  Brain       Date:  2009-03-02       Impact factor: 13.501

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

4.  Affiliative behavior in Williams syndrome: social perception and real-life social behavior.

Authors:  Anna Järvinen-Pasley; Ralph Adolphs; Anna Yam; Kiley J Hill; Mark Grichanik; Judy Reilly; Debra Mills; Allan L Reiss; Julie R Korenberg; Ursula Bellugi
Journal:  Neuropsychologia       Date:  2010-04-10       Impact factor: 3.139

5.  The 7q11.23 Protein DNAJC30 Interacts with ATP Synthase and Links Mitochondria to Brain Development.

Authors:  Andrew T N Tebbenkamp; Luis Varela; Jinmyung Choi; Miguel I Paredes; Alice M Giani; Jae Eun Song; Matija Sestan-Pesa; Daniel Franjic; André M M Sousa; Zhong-Wu Liu; Mingfeng Li; Candace Bichsel; Marco Koch; Klara Szigeti-Buck; Fuchen Liu; Zhuo Li; Yuka I Kawasawa; Constantinos D Paspalas; Yann S Mineur; Paolo Prontera; Giuseppe Merla; Marina R Picciotto; Amy F T Arnsten; Tamas L Horvath; Nenad Sestan
Journal:  Cell       Date:  2018-11-01       Impact factor: 41.582

Review 6.  Animal models of Williams syndrome.

Authors:  Lucy R Osborne
Journal:  Am J Med Genet C Semin Med Genet       Date:  2010-05-15       Impact factor: 3.908

7.  Genetic mapping of brain plasticity across development in Williams syndrome: ERP markers of face and language processing.

Authors:  D L Mills; L Dai; I Fishman; A Yam; L G Appelbaum; M St George; A Galaburda; U Bellugi; J R Korenberg
Journal:  Dev Neuropsychol       Date:  2013       Impact factor: 2.253

8.  Visuospatial interpolation in typically developing children and in people with Williams Syndrome.

Authors:  Melanie Palomares; Barbara Landau; Howard Egeth
Journal:  Vision Res       Date:  2008-09-27       Impact factor: 1.886

Review 9.  Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior.

Authors:  Anna Järvinen-Pasley; Ursula Bellugi; Judy Reilly; Debra L Mills; Albert Galaburda; Allan L Reiss; Julie R Korenberg
Journal:  Dev Psychopathol       Date:  2008

10.  Visual phenotype in Williams-Beuren syndrome challenges magnocellular theories explaining human neurodevelopmental visual cortical disorders.

Authors:  Miguel Castelo-Branco; Mafalda Mendes; Ana Raquel Sebastião; Aldina Reis; Mário Soares; Jorge Saraiva; Rui Bernardes; Raquel Flores; Luis Pérez-Jurado; Eduardo Silva
Journal:  J Clin Invest       Date:  2007-12       Impact factor: 14.808

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