You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 46 No. 12, December 1989 TABLE OF CONTENTS
  Archives
  •  Online Features
  LETTERS TO THE EDITOR
 This Article
 •References
 •Full text PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati Add to Twitter What's this?

Fragile X Syndrome: A Genetic Etiology for Developmental Gerstmann's Syndrome

JiM Grigsby, PhD
Rocky Mountain Multiple Sclerosis Center PO Box 2901, Dept 7500 Englewood, CO 80110

Randi Hagerman, MD
Child Development Unit Children's Hospital 1056 E 19th Ave Denver, CO 80218

Arch Neurol. 1989;46(12):1269-1270.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

To the Editor.

—We read with interest the recent article by PeBenito et al1 of several cases of developmental Grestmann's syndrome. We were concerned that mention was not made of fragile X syndrome as a possible cause. The validity of Gerstmann's syndrome,2,3 which is comprised of dysgraphia, dyscalculia, finger agnosia, and right-left disorientation, has been the subject of considerable debate.4-10 The same has been true of the developmental Gerstmann syndrome (DGS), which also includes deficits in constructional praxis.11,12

PeBenito et al reported on five children who had all five signs of the developmental Gerstmann disorder, as well as various combinations of motor and attentional problems. Four of the five had at least average reading ability. In their discussion, the authors state that "the etiology of DGS is unknown. Whereas some specific learning disorders (eg, dyslexia) have a familial tendency, this is not observed in DGS" (p . . . [Full Text PDF of this Article]



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1989 American Medical Association. All Rights Reserved.