Bone mineral density (BMD) was evaluated in the proximal femora (femoral neck, Ward's triangle, and greater trochanter) and lumbar spines of 25 black children and young adults with sickle cell anemia using dual-photon absorptiometry. Compared with normal subjects from the general population, the patients with sickle cell anemia exhibited lower bone mineral density values in all scan regions (approximately 6% to 21% lower than expected). These differences in the lumbar spine were significant for both girls and boys. When compared with normal black subjects from the general population, the girls with sickle cell anemia exhibited significantly lower lumbar spine bone mineral density, and the boys with sickle cell anemia exhibited significantly...
Copyright © 2012 Ibrahim Aslan et al. This is an open access article distributed under the Creative ...
Aim. We assessed the bone mineral density and related parameters in nine adults, thirty-eight pubert...
Aim: Fragile bones develop due to various factors in thalassemic patients. Even with optimum managem...
Sickle cell anemia and thalassemia result in impaired bone health in both adults and youths. Childre...
ABSTRACT. Objective. Children with sickle cell dis-ease (SCD) experience poor growth, altered body c...
Background Adult patients with sickle-cell disease (SCD) often have multiple bone compactions causin...
Objectives (background): Both sickle cell disease and vitamin D deficiency are common among Saudi p...
OBJECTIVES: To determine whether kidney disease and hemolysis are associated with bone mass density ...
Background: Sickle cell anemia is the most common genetic disease in sub-Saharan Africa. It is an in...
Sickle bone disease (SBD) is a chronic and invalidating complication of Sickle cell disease (SCD), a...
In sickle cell disease, erythroid hyperplasia causes trabecular destruction leading to low bone dens...
Abstract Background: Beta-thalassemia is an autosomal recessive hemoglobinopathy with frequent skel...
Management of thalassemia major has shown substantial clinical and prognostic improvement, suggestin...
Introdução: A doença falciforme (DF) é a hemoglobinopatia mais comum no mundo, e geralmente é assoc...
The growth status of 46 American Black children with sickle-cell anemia (SS) and 26 children with si...
Copyright © 2012 Ibrahim Aslan et al. This is an open access article distributed under the Creative ...
Aim. We assessed the bone mineral density and related parameters in nine adults, thirty-eight pubert...
Aim: Fragile bones develop due to various factors in thalassemic patients. Even with optimum managem...
Sickle cell anemia and thalassemia result in impaired bone health in both adults and youths. Childre...
ABSTRACT. Objective. Children with sickle cell dis-ease (SCD) experience poor growth, altered body c...
Background Adult patients with sickle-cell disease (SCD) often have multiple bone compactions causin...
Objectives (background): Both sickle cell disease and vitamin D deficiency are common among Saudi p...
OBJECTIVES: To determine whether kidney disease and hemolysis are associated with bone mass density ...
Background: Sickle cell anemia is the most common genetic disease in sub-Saharan Africa. It is an in...
Sickle bone disease (SBD) is a chronic and invalidating complication of Sickle cell disease (SCD), a...
In sickle cell disease, erythroid hyperplasia causes trabecular destruction leading to low bone dens...
Abstract Background: Beta-thalassemia is an autosomal recessive hemoglobinopathy with frequent skel...
Management of thalassemia major has shown substantial clinical and prognostic improvement, suggestin...
Introdução: A doença falciforme (DF) é a hemoglobinopatia mais comum no mundo, e geralmente é assoc...
The growth status of 46 American Black children with sickle-cell anemia (SS) and 26 children with si...
Copyright © 2012 Ibrahim Aslan et al. This is an open access article distributed under the Creative ...
Aim. We assessed the bone mineral density and related parameters in nine adults, thirty-eight pubert...
Aim: Fragile bones develop due to various factors in thalassemic patients. Even with optimum managem...