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Sickle cell anemia: A review of the dental concerns and a retrospective study of dental and bony changes
Authors:Lincoln B. Taylor DDS  MS    Arthur J. Nowak DMD    Roger H. Giller MD   Paul S. Casamassimo DDS  MS
Affiliation:assistant professor of pediatric dentistry, University of Tennessee, Dunn Dental Building, Memphis, Tennessee;professor of pediatric dentistry and pediatrics, University of Iowa, College of Dentistry, Iowa City, Iowa.;associate professor of pediatrics, University of Colorado School of Medicine, Division of Hematology, Oncology &Bone Marrow Transplant, The Children's Hospital, Denver;professor and chairman of pediatric dentistry, Children's Hospital, Columbus, Ohio
Abstract:
This paper is a review of the medical concerns pertinent to dental care and a preliminary study of dental findings of the sickle cell anemia (SS) patient. The dental characteristics observed in 21 dental patients with SS are described. Radiographic findings included "stepladder" trabeculae pattern (70%), enamel hypomineralization (24%), calcified canals (5%), Increased overbite (30–80%), and increased overjet (56%). Comparisons are made with other studies of the sickle cell patient, and the need for further study is suggested.
Keywords:
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