Sentences with phrase «as sickle cell anemia»

Because anemia has to do with the blood, it is sometimes a symptom of another underlying health issue or as a symptom of a blood disease such as sickle cell anemia.

When blood cell production is interrupted by disease, cancers (such as leukemia) or genetic abnormalities (such as sickle cell anemia), a person...

Low plasma levels of zinc have been observed in congenital diseases such as sickle cell anemia (Ballester et al. 1986), Down's syndrome (Licastro et al. 1992) and acrodermatitis enteropathica.

However, keep ALL iron supplements away from children, even carbonyl iron, and do not take any kind of iron supplement if you have hemochromatosis, hemosiderosis or hemolytic anemia such as sickle cell anemia or thalassemia (aka Mediterranean anemia, a type of genetic anemia where hemoglobin is not well formed)

Carrier screening for hemoglobinopathies such as sickle cell anemia is recommended by the American Congress of Obstetricians and Gynecologists (ACOG) via complete blood count and hemoglobin electrophoresis for people of African, Southeast Asian, Mediterranean, Middle Eastern, and West Indian descent considering having children.

An authority on the study and treatment of childhood cancers, as well as the biology and therapy of hemoglobinopathies — blood diseases such as sickle cell anemia and thalassemia — Cunningham is known for his work on understanding the molecular mechanism underpinning red blood cell production.

Along with his colleagues, Shaqfeh has now created the first simplified computer model of the process that forms that layer — a model that could help to improve the design of artificial platelets and medical treatments for trauma injuries and for blood disorders such as sickle cell anemia and malaria.

Because the deformation of red blood cells is a key factor in the Fåhræus - Lindqvist layer, its properties are altered in diseases, such as sickle cell anemia, that affect the shape and rigidity of those cells.

Other plans include using CRISPR to reverse blood disorders, such as sickle cell anemia and beta thalassemia, caused by mutations in the hemoglobin gene.

Not exact matches

As early as the first trimester, doctors can take a sample of placental tissue (chorionic villus sampling, or CVS) to detect whether a baby has the genes that would lead to sickle cell anemia or sickle cell traiAs early as the first trimester, doctors can take a sample of placental tissue (chorionic villus sampling, or CVS) to detect whether a baby has the genes that would lead to sickle cell anemia or sickle cell traias the first trimester, doctors can take a sample of placental tissue (chorionic villus sampling, or CVS) to detect whether a baby has the genes that would lead to sickle cell anemia or sickle cell trait.

Cord blood transplants are also accepted as treatment for thalassemia and sickle cell anemia, inherited blood disorders that are prevalent in certain ethnic groups.

Choose an obstetrician or health care provider Interview potential doctors Contact health insurance company about coverage Start and pregnancy and birth budget Discuss financial effects of pregnancy and baby with partner Stop smoking Stop drinking Stop using street drugs Talk to your physician about any prescription medications Drink at least 8 glasses of water every day Visit the doctor at least once per month or every 4 weeks Do not dye or perm hair Stop drinking coffee and other caffeinated beverages Exercise daily Start taking prenatal vitamins Eat foods rich in folic acid Eat iron rich foods Increase daily intake of whole grains, fruits and vegetables Nap as much as possible as fatigue is common Eat fish with low levels of mercury no more than 2 days per week Do not eat undercooked meats Do not eat unpasteurized dairy producs Do not eat cold cut deli meats Allow someone else to clean out the kitty litter, if applicable Limit exposure to chemicals Try to limit stress and tension Complete all prenatal tests — HIV, Chlamydia, Gonorrhea, Anemia, Blood Typing, Sickle Cell Anemia, Urine Screening and Rubella.

Tomorrow, September 30, join Preserve Our Legacy Inc. as they host a fundraising event for young people afflicted with sickle cell anemia.

Harvard Stem Cell Institute (HSCI) scientists have taken the first steps toward developing a treatment that would make bone marrow — blood stem cell — transplantation safer and, as a result, more widely available to the millions of people living with blood disorders like sickle cell anemia, thalassemia, and ACell Institute (HSCI) scientists have taken the first steps toward developing a treatment that would make bone marrow — blood stem cell — transplantation safer and, as a result, more widely available to the millions of people living with blood disorders like sickle cell anemia, thalassemia, and Acell — transplantation safer and, as a result, more widely available to the millions of people living with blood disorders like sickle cell anemia, thalassemia, and Acell anemia, thalassemia, and AIDS.

The primary cause of anemia is iron deficiency, but it can co-occur with other conditions, such as malaria and genetic disorders like sickle cell.

No one denies that some groups are more vulnerable than others to certain disorders, such as sickle - cell anemia, and thus knowing someone's race or ethnicity can be as pertinent to diagnosis as knowing their sex.

Stem cell treatments are already a reality for diseases of the blood, such as leukemia and sickle - cell anemia (like Paizley's), and for tissue repair of the skin and the cornea.

Only a handful of states have outlawed discrimination based on genetic testing, and most laws are aimed at specific tests, such as one for sickle cell anemia.

On the other end of the spectrum are Mendelian diseases such as cystic fibrosis and sickle - cell anemia, which are caused by abnormalities to a single gene.

Gene editing techniques have the potential to treat blood disorders that run in families, such as thalassemia and sickle cell anemia, but their application has been largely limited to cells in a laboratory and not living animals.

«The study indicates that screening for silent strokes in children starting school can lead to early detection and prevention of recurrences as well as reduction in other complications of sickle cell anemia such as acute painful episodes and acute chest syndrome.

Vanderbilt - led research, as part of an international, multicenter trial, found regular blood transfusion therapy significantly reduces the recurrence of silent strokes and strokes in children with sickle cell anemia who have had pre-existing silent strokes, according to study results released today in the New England Journal of Medicine (NEJM).

A number of new clinical trials aim to take cells from a patient, such as blood cells or immune cells, edit them and transfer them back with new power to undermine diseases like cancer or sickle cell anemia.

She also worked as a consultant in Washington for the Job Corps Sickle Cell Anemia Program.

He and other supporters argued unsuccessfully that the move would pave the way to cures for conditions such as spinal cord injuries and sickle - cell anemia as well as degenerative disorders such as multiple sclerosis and Parkinson's and Alzheimer's diseases.

Soon after birth, a baby's blood is sampled and tested for a number of rare inherited conditions, such as cystic fibrosis and sickle cell anemia.

«The one thing that I think that is useful is maybe when people write knockout papers they might describe the housing conditions in more detail,» says Chris Paszty, scientific director at the biotech company Amgen, Inc., headquartered in Thousand Oaks, Calif., who as a postdoctoral researcher at Lawrence Berkeley National Laboratory developed a mouse model for the study of sickle cell anemia.

These mice have their hemoglobin genes removed and replaced with the mutated human version, saddling them with many of the same problems as human sufferers, including immature, short - lived, and sickle - shaped red blood cells; anemia; reduced blood flow; and an enlarged spleen.

«If carriers are more likely to survive and reproduce, then evolutionary pressure might favor carriers in the long term, as is seen for sickle cell anemia and malaria infection.»

Along with treating children with malignant disease, he also will care for those whose blood disorders are not malignant, such as patients with sickle cell anemia.

What's more, inherited diseases can arise from a problem with one gene (a simple example is sickle - cell anemia, a condition caused by defects in a single gene that makes the hemoglobin protein), or from interactions among a range of genetic variations as well as, frequently, environmental stresses.

In contrast to Mendelian disorders (e.g., Huntington's disease, sickle cell anemia) in which variation in a single gene causes disease, common complex disorders, such as heart disease, diabetes, and most cancers, develop as a result of both genetic and environmental factors.

These advances make it possible for half - identical bone marrow transplants to be used in nonmalignant diseases, such as aplastic anemia, lupus, and sickle cell anemia.

The process, known as prenatal screening, is already used to determine whether an embryo exhibits signs of conditions like Down syndrome and diseases like sickle cell anemia, but it could also be used to identify any other genetic abnormalities — particularly genetic mutations — exhibited by an embryo.

When a couple is known to be at risk for having a child with a specific genetic disorder, such as cystic fibrosis or sickle cell anemia, the woman undergoes a procedure to remove some eggs.

Generally, a hematologist treats patients with blood disorders, such as types of hemophilia, leukemia, lymphoma, and sickle cell anemia.

Just as children of Jewish descent are more likely to have Tay Sachs disease and African Americans are more likely to have sickle cell anemia, so children with certain characteristics are at greater risk of becoming jaundiced.

Been diagnosed with, been treated for or advised by a licensed member of the medical profession to receive treatment for Alzheimer's, dementia, memory loss, organic brain disease, mental incapacity, Lou Gehrig's disease (ALS), Down's Syndrome, Huntington's disease, sickle cell anemia, cystic fibrosis, cerebral palsy or been diagnosed by a medical professional as having a terminal medical condition that is expected to result in death within the next 18 months?

If you were dealing with a company that asks about sickle cell anemia and you have filled a prescription for Hydroxyurea, they would absolutely view you as a SCD patient.

Has the Proposed Insured been medically diagnosed as having cerebral palsy, muscular dystrophy, cystic fibrosis, sickle cell anemia, Down's syndrome or congenital heart disease?

Cord blood has been studied extensively for the treatment of hematological diseases such as cancer and sickle cell anemia, but is now in phase II trials for the alleviation of autism.