The clinical significance of congenital Agenesis of the Corpus Callosum

Erin D. Bigler; Leslie D. Rosenstein; Mary Roman; Nancy L. Nussbaum

doi:10.1016/0887-6177(88)90063-7

The clinical significance of congenital Agenesis of the Corpus Callosum

Erin D. Bigler, Leslie D. Rosenstein, Mary Roman, Nancy L. Nussbaum

Research output: Contribution to journal › Article › peer-review

8 Scopus citations

Abstract

Three cases of congenital agenesis of the corpus callosum (ACC) are presented along with typical clinical features observed on computerized tomography and magnetic resonance imaging. Most congenital ACC cases do not display hemisyndromes or callosal syndromes, but do exhibit some deficit in terms of hemispheric integration. The most common neuropsychological impairments are in the areas of motor and perceptual-motor functioning. Clinical guidelines in the assessment of ACC patients are given.

Original language	English (US)
Pages (from-to)	189-200
Number of pages	12
Journal	Archives of Clinical Neuropsychology
Volume	3
Issue number	2
DOIs	https://doi.org/10.1016/0887-6177(88)90063-7
State	Published - 1988

ASJC Scopus subject areas

Neuropsychology and Physiological Psychology
Clinical Psychology
Psychiatry and Mental health

Access to Document

10.1016/0887-6177(88)90063-7

Cite this

@article{404553f325eb4ebab7504586b08802a6,

title = "The clinical significance of congenital Agenesis of the Corpus Callosum",

abstract = "Three cases of congenital agenesis of the corpus callosum (ACC) are presented along with typical clinical features observed on computerized tomography and magnetic resonance imaging. Most congenital ACC cases do not display hemisyndromes or callosal syndromes, but do exhibit some deficit in terms of hemispheric integration. The most common neuropsychological impairments are in the areas of motor and perceptual-motor functioning. Clinical guidelines in the assessment of ACC patients are given.",

author = "Bigler, {Erin D.} and Rosenstein, {Leslie D.} and Mary Roman and Nussbaum, {Nancy L.}",

year = "1988",

doi = "10.1016/0887-6177(88)90063-7",

language = "English (US)",

volume = "3",

pages = "189--200",

journal = "Archives of Clinical Neuropsychology",

issn = "0887-6177",

publisher = "Elsevier BV",

number = "2",

}

TY - JOUR

T1 - The clinical significance of congenital Agenesis of the Corpus Callosum

AU - Bigler, Erin D.

AU - Rosenstein, Leslie D.

AU - Roman, Mary

AU - Nussbaum, Nancy L.

PY - 1988

Y1 - 1988

N2 - Three cases of congenital agenesis of the corpus callosum (ACC) are presented along with typical clinical features observed on computerized tomography and magnetic resonance imaging. Most congenital ACC cases do not display hemisyndromes or callosal syndromes, but do exhibit some deficit in terms of hemispheric integration. The most common neuropsychological impairments are in the areas of motor and perceptual-motor functioning. Clinical guidelines in the assessment of ACC patients are given.

AB - Three cases of congenital agenesis of the corpus callosum (ACC) are presented along with typical clinical features observed on computerized tomography and magnetic resonance imaging. Most congenital ACC cases do not display hemisyndromes or callosal syndromes, but do exhibit some deficit in terms of hemispheric integration. The most common neuropsychological impairments are in the areas of motor and perceptual-motor functioning. Clinical guidelines in the assessment of ACC patients are given.

UR - http://www.scopus.com/inward/record.url?scp=0023730649&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0023730649&partnerID=8YFLogxK

U2 - 10.1016/0887-6177(88)90063-7

DO - 10.1016/0887-6177(88)90063-7

M3 - Article

C2 - 14591270

AN - SCOPUS:0023730649

SN - 0887-6177

VL - 3

SP - 189

EP - 200

JO - Archives of Clinical Neuropsychology

JF - Archives of Clinical Neuropsychology

IS - 2

ER -

The clinical significance of congenital Agenesis of the Corpus Callosum

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this