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 JAMA
Advanced Search

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


  Vol. 269 No. 24, June 23, 1993 TABLE OF CONTENTS
  JAMA
  •  Online Features
  Grand Rounds at the Clinical Center of the National Institutes of Health
 This Article
 •References
 •Full text PDF
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Contact me when this article is cited
 Related Content
 •Similar articles in JAMA
 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?

Hereditary Hemochromatosis

Tracey A. Rouault, MD

JAMA. 1993;269(24):3152-3154.

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

SELECTED CASE

A 44-year-old man had shoulder and finger pain and consulted his local physician. Screening blood tests were obtained as part of the initial evaluation and revealed the following values: hemoglobin, 135 g/L; hematocrit, 0.40; serum iron, 37 µmol/L (209 µg/dL); transferrin, 2.19 g/L; transferrin saturation, 95%; and serum ferritin, 2430 µg/L. Liver function tests revealed the following values: aspartate aminotransferase, 43 U/L; alanine aminotranferase, 68 U/L; and alkaline phosphatase and bilirubin, normal. A liver biopsy was performed and examination of tissue sections revealed fatty metamorphosis and an increase in fibrous tissue in portal areas consistent with early cirrhosis. Large amounts of parenchymal iron were noted on Prussian blue staining, particularly in the periportal area.

The diagnosis based on the test results was hemochromatosis, and a phlebotomy program was initiated. The patient was referred to the National Institutes of Health where on physical examination the absence of frank arthritis . . . [Full Text PDF of this Article]


Author Affiliations

From the Cell Biology and Metabolism Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Md.


Footnotes

Reprint requests to National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892 (Dr Rouault).



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
 
© 1993 American Medical Association. All Rights Reserved.