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. 148 No. 4, April 1994 TABLE OF CONTENTS
  Archives
  •  Online Features
  Pediatric Forum
 This Article
 •References
 •Full text PDF
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •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?

Hypothyroidism in Patients With Down Syndrome

Clare Mitchell, MD; Jean Blachford, MD; M. Joyce Carlyle, MD, FRCP
Department of Pediatrics Child and Parent Resource Institute 600 Sanatorium Rd London, Ontario, Canada N6H 3W7 C. Clarson, FRCP Department of Pediatrics University of Western Ontario London, Ontario, Canada N6C 2V5

Arch Pediatr Adolesc Med. 1994;148(4):441-442.

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

Acquired hypothyroidism is more common in children with Down syndrome than in other children. In children without Down syndrome, acquired hypothyroidism is rare before age 3 years and is not reported to occur frequently until adolescence.1 Previous reports of hypothyroidism in children with Down syndrome have described onset at a similar age. Postneonatal-onset hypothyroidism in the very young children with Down syndrome described herein has not previously been reported, to our knowledge.

At the Child and Parent Resource Institute in London, Ontario, we have a multidisciplinary outpatient developmental program for children with Down syndrome. At the time of this writing, we had approximately 120 children aged between 6 weeks and 17 years in the program.

Patient Reports.Patient 1. This 61/2-month-old female infant was born at 37 weeks' gestation to a 39-year-old mother who had a distant family history of thyroid disease. The mother and father were third cousins. . . . [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 | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1994 American Medical Association. All Rights Reserved.