Cdc hemoglobinopathy fact sheet

Sickle cell disease (SCD) is a common inherited blood disorder in the United States, affecting an estimated 70,000 to 100,000 Americans. SCD can lead to lifelong disabilities and reduce average life expectancy.

PHRESH - Public Health Research Epidemiology Surveillance. The California PHRESH Project is a two-year project funded by the Centers for Disease Control and Prevention. PHRESH stands for the Public Health, Research, Epidemiology & Surveillance in Hemoglobinopathies. Project Objectives:

ACT Sheets. ACT Sheets or ACTion sheets are action plans for each disorder that provide recommended immediate next steps for a health professional to follow when a newborn has an out-of-range test result. Hemoglobin E disease is not a form of sickle cell disease. People with hemoglobin E disease normally do not have serious medical problems related to the disease. People with hemoglobin E disease may have mild anemia. What if both parents have hemoglobin E trait? If both parents have hemoglobin E trait there is a 25 percent (1 in 4) chance with ... Hemoglobin E disease is not a form of sickle cell disease. People with hemoglobin E disease normally do not have serious medical problems related to the disease. People with hemoglobin E disease may have mild anemia. What if both parents have hemoglobin E trait? If both parents have hemoglobin E trait there is a 25 percent (1 in 4) chance with ... Hemoglobinopathies is the medical term for a group of blood disorders and diseases that affect red blood cells. These disorders include both sickle cell disease (SCD) and thalassemia. Hemoglobinopathies monitoring means finding out the number of people with these conditions and how having a ... Hemoglobin E disease is not a form of sickle cell disease. People with hemoglobin E disease normally do not have serious medical problems related to the disease. People with hemoglobin E disease may have mild anemia. What if both parents have hemoglobin E trait? If both parents have hemoglobin E trait there is a 25 percent (1 in 4) chance with ...

Newborn Screening ACT Sheet . FC (HbCC Disease or HbC/Beta Zero Thalassemia) HbC/β0 Disease. Differential Diagnosis: Homozygous hemoglobin C, hemoglobin C/beta zero (β0) thalassemia, or hereditary persistence of fetal hemoglobin (Hb C/HPFH). Condition Description: An uncommonred blood cell disorder characterized by presence of fetal hemoglobin Your patient has tested positive for hemoglobin C trait. Hemoglobin C trait is not disease and is not associated with anemia or other disease medical issues. Although hemoglobin C trait has no immediate clinical significance, this information is important for future reproductive decisions of the child and other family members. In 2010, the Registry and Surveillance System for Hemoglobinopathies (RuSH) pilot project was implemented by the Centers for Disease Control and Prevention (CDC) to collect state-specific, population-based data on people with sickle cell disease (SCD... NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health. ACMG ACT Sheets and Confirmatory Algorithms [Internet]. Bethesda (MD): American College of Medical Genetics; 2001 ... Hemoglobin D or G trait is not disease and is not associated with anemia or other disease medical issues. ... Please give the enclosed parent fact sheet to your patient.