Please use this identifier to cite or link to this item:
|Title:||Zinc, copper and iron and their interrelations in the growth of sickle cell patients|
|Authors:||Braga, Josefina Aparecida Pellegrini [UNIFESP]|
Kerbauy, José [UNIFESP]
Fisberg, Mauro [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
|Publisher:||Archivos Latinoamericanos Nutricion|
|Citation:||Archivos Latinoamericanos De Nutricion. Caracas: Archivos Latinoamericanos Nutricion, v. 45, n. 3, p. 198-203, 1995.|
|Abstract:||In this study we evaluated the nutritional status of 34 children with sickle cell disease (SS). Results were compared to 9 siblings with sickle cell trait (AS) and 35 eutrophic children who presented normal hemoglobin and normal hemoglobin electrophoresis (AA). All of then came from low socioeconomic level.Analysis of the growth velocity curves revelead in SS group, tendency to increase deficit in weight and height with age. There was no relation between weight/height (W/H) and height/age (H/A) percentile and hemoglobin levels. There was no significant relation between nutritional status and severity of the disease. SS group showed significant skeletal maturation delay, the same did not occur with the siblings (AS group).Plasma zinc levels were significantly lower in SS group than in AS and AA groups In SS group there was some association between lower plasma zinc levels and WA percentile lower or equal to 10. Plasma copper levels were significantly greater in SS group than in AS and AA ones, and then was no relation between plasma copper levels and serum ferritin levels.In conclusion, our patients with sickle cell disease showed indexes of malnutrition, iron deficiency, hipercupremia and low plasma zinc levels related to low stature.|
|Appears in Collections:||Artigo|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.