Century of Progress: Milestones in Sickle Cell Disease
Diana, Princess of Wales Me…This study investigated the prevalence of dental caries and periodontal condition in a population with sickle cell disease (SCD), analyzing some associations with disease severity. The Decayed, Missing and Filled Teeth index (DMFT) and Community Periodontal Index (CPI) were recorded for 99 individuals with SCD and 91 matched controls. Socio-demographic status, oral health behaviors, and The study evaluated 42 patients, mean age 36 years (range: 18–53 years), with sickle cell anemia or HbSß 0 thalassemia who were treated with hydroxyurea and were followed for a mean of 6.6 years. The study by Rothman et al [13] enrolled 37 patients in the hydroxyurea arm and administered 25.2 (+/− 5.6) mg/kg/day of hydroxyurea.The purpose of this cohort study was to determine whether individuals with sickle cell anemia (SCA) were more susceptible to dental caries than non-sickle-cell control subjects. A review of the literature suggests several reasons why individuals with SCA may be at increased risk. Thirty-five cases of SCA aged 6 years and older were identified 20.02.2020 · Sickle cell disease (SCD) results in chronic hemolytic anemia, recurrent vascular occlusion, insidious vital organ deterioration, early mortality, and diminished quality of life. Life-threatening acute physiologic crises may occur on a background of progressive diminishing vital organ function. Sickle hemoglobin polymerizes in the deoxygenated state, resulting in erythrocyte membrane
Dental health in sickle cell disease - OAText
20.10.2018 · Sickle cell disease (SCD) is the most prevalent monogenic hereditary pathology associated with the presence of hemoglobin SS in the world. It can affect individuals, leading to changes in the face and body, causing a deficiency in dental and bone tissue formation that can ultimately result in a higher level of predisposition to developing dental caries.01.12.2011 · 78. Laurence B, et al. Sickle cell anemia and dental caries: A literature review and pilot study. Spec Care Dentist 2002;22:70-74. 79. Marti-Carvajal AJ, et al. Treatment for avascular necrosis of bone in people with sickle cell disease. Cochrane Database …01.07.2001 · Sickle cell anemia (SCA) is a hemolytic anemia characterized by abnormally shaped (sickled) red blood cells (RBCs), which are removed from the circulation and destroyed at increased rates, leading to anemia. Of greater clinical importance, the sickled RBCs cause vascular occlusion, which leads to tissue ischemia and infarction.This course is designed to provide an overview on epidemiology and the Internet for medical and health related students around the world based on the concept of Global Health Network University and Hypertext Comic Books.Sickle cell disease (SCD) is a group of blood disorders typically inherited from a person's parents. The most common type is known as sickle cell anaemia (SCA). It results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells. This leads to a rigid, sickle-like shape under certain circumstances. Problems in sickle cell disease typically begin around 5 to 6
(PDF) Bone involvement in sickle cell disease | Antonio
12.03.2008 · The purpose of this cohort study was to determine whether individuals with sickle cell anemia (SCA) were more susceptible to dental caries than non‐sickle‐cell control subjects. A review of the literature suggests several reasons why individuals with SCA may be at increased risk.12.08.2020 · Sickle cell anemia and dental caries: a literature review and pilot study. Special Care in Dentistry: Official Publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry. 2002;22(2): 70 – 74. Epub 2002/07/12.review Bone involvement in sickle cell disease Antonio Almeida and Irene Roberts Department of Haematology, Imperial College London, Hammersmith Hospital, London, UK occlusion, the hallmark of the painful sickle cell crisis, is Summary complex involving activation and adhesion of leucocytes, Bone involvement is the commonest clinical manifestation of platelets and endothelial cells as well as No statistically significant differences were found in the prevalence or severity of caries between subjects with SCD and those without SCD as measured by the DMFT index and its component scores.In 2002, our research group compared 35 dental patients with SCA, aged 6 years and older, to 140 dental patients who did not have anemia (in a 4:l age-, gender-matched study) to determine whether 29.01.2012 · 52. Laurence B, et al. Sickle cell anemia and dental caries: A literature review and pilot study. Spec Care Dentist 2002;22:70-74. 53. Richards LH, et al. Community-acquired Salmonella bacteraemia in patients with sickle-cell disease 1969-2008: A single centre study. Scand J Infect Dis 2011;43:89-94. 54.
Anemia and Dental Caries in Pregnant Women: a Prospective
Research conducted using data from patients enrolled in the Cooperative Study of Sickle Cell Disease shows that the chances of having a cerebrovascular accident (defined as transient ischemic attack, completed infarctive stroke, and hemorrhagic stroke) for the first time by age 20 years is 11 percent and by age 45 years is 24 percent for those with HbSS (i.e., the form of SCD in which a child 12.03.2008 · The purpose of this cohort study was to determine whether individuals with sickle cell anemia (SCA) were more susceptible to dental caries than non-sickle-cell control subjects. A review of the literature suggests several reasons why individuals with SCA may be at increased risk. Thirty-five cases of SCA aged 6 years and older were identified 07.04.2021 · Thalassemia is a hematologic disorder caused by genetic mutation resulting in impaired hemoglobin chain production. Patients with thalassemia commonly experience complications such as anemia, blood transfusion-related issues, hepatic or cardiac involvement, and psychosocial impacts. Rarely, priapism has been associated with thalassemia as an initial presentation or subsequently …Sickle cell disease, also known as sickle cell anemia, is inherited. People who have the disease inherit two copies of the sickle cell gene—one from each parent. The gene codes for production of an abnormal hemoglobin. If a person inherits only one copy of the sickle cell gene, he or she will have sickle cell trait.20.05.2020 · Sickle cell anemia (SCA) was first described in the Western literature more than 100 years ago. Elucidation of its molecular basis prompted numerous biochemical and genetic studies that have contributed to a better understanding of its pathophysiology. Unfortunately, the translation of such knowledge into developing treatments has been disproportionately slow and elusive.
Supercourse: Epidemiology, the Internet, and Global Health
Sickle cell anemia, a genetic disease caused by a mutation in the beta-globin gene, can present oral manifestations such as delayed tooth eruption and hypomineralized enamel and dentin. The aim of the present study was to evaluate the prevalence and severity of developmental defects of enamel (DDE) and delayed tooth eruption in children with sickle cell anemia.07.12.2020 · Intrinsic tooth discoloration is reported in patients with blood dyscrasias such as sickle cell anemia, thalassemia, and HDN. These diseases have the potential to cause hemolysis and the subsequent dose-dependent incorporation of biliverdin (by-product pigment of bilirubin) into developing teeth, producing a jaundicelike yellow-green tint on the tooth surfaces.The purpose of this cohort study was to determine whether individuals with sickle cell anemia (SCA) were more susceptible to dental caries than non-sickle-cell control subjects. A review of the literature suggests several reasons why individuals with SCA may be at increased risk. Thirty-five cases o …Dental caries cavities or holes in Sickle cell anemia Systematic review a structured review of the literature designed to answer a clearly formulated question. Systematic reviews use systematic and explicitly predetermined methods to identify, select and critically evaluate research relevant to …Sickle cell disease, also known as sickle cell anemia, is inherited. People who have the disease inherit two copies of the sickle cell gene—one from each parent. The gene codes for production of an abnormal hemoglobin. If a person inherits only one copy of the sickle cell gene, he or she will have sickle cell trait.
No comments:
Post a Comment