Bibliographic Details
Title: |
Chediak–Higashi syndrome in the intensive care unit. |
Authors: |
Demirkiran, Oktay1 odemirkiran@superonline.com, Utku, Tughan1, Urkmez, Seval1, Dikmen, Yalim1 |
Source: |
Pediatric Anesthesia. Aug2004, Vol. 14 Issue 8, p685-688. 4p. |
Subject Terms: |
*INTENSIVE care units, *PEDIATRIC anesthesia, *INFECTION, *CYTOPLASMIC granules, *ALBINISM, *HEMORRHAGE, *POSTOPERATIVE period |
Abstract: |
Chediak–Higashi Syndrome is a rare autosomal recessive disease characterized by recurrent infections, giant cytoplasmic granules and oculocutaneous albinism. We describe the clinical and laboratory findings of a patient with Chediak–Higashi syndrome who was diagnosed and treated in the intensive care unit because of bleeding tendency after surgery. [ABSTRACT FROM AUTHOR] |
|
Copyright of Pediatric Anesthesia is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) |
Database: |
Academic Search Complete |