[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 54.163.94.5. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Article
June 1988

Snoring, Daytime Sleepiness, and Sickle Cell Anemia

Author Affiliations

Sleep Disorders Center Henry Ford Hospital 22921 W Grand Blvd Detroit, MI 48202
Department of Pharmacy University of Michigan Medical Center Ann Arbor, MI 48109
Comprehensive Sickle Cell Center Children's Hospital of Michigan 3901 Beaubien Blvd Detroit, MI 48201

Am J Dis Child. 1988;142(6):589. doi:10.1001/archpedi.1988.02150060023008
Abstract

Sir.—Theoretically, in patients with sickle cell anemia who autosplenectomize by age 4 to 5 years a compensatory hyperplasia of other lymphoid organs may develop, particularly in the tonsils and adenoids. If so, symptoms associated with tonsillar hyperplasia should occur more often in patients with sickle cell disease than in normal children. Enlarged tonsils and adenoids are the most frequent cause of sleep apnea syndrome in pediatric patients.1 If tonsillar and adenoidal hypertrophy is more common in patients with sickle cell disease than in children without the disease, the symptoms of sleep apnea syndrome (eg, snoring and daytime sleepiness) should occur more frequently in them than in children without this disease. Since hypoxemia is poorly tolerated by patients with sickle cell anemia, sleep-related apnea in this population could produce much greater morbidity than in children with normal oxygen transport. In particular, sleep-related hypoxemia could possibly precipitate the various acute

First Page Preview View Large
First page PDF preview
First page PDF preview
×