sickle cell anaemia BrE
sickle cell anemia AmE
sickle cell disease
sickle cell disorder
sickle cell syndrome , także: sickle-cell anaemia BrE , także: sickle-cell anemia AmE , także: sickle-cell disease , także: sickle-cell disorder , SCD (skrót)

In the continental zone, sickle cell anaemia is common.

Chronic and acute problems associated with sickle cell anaemia.

He also studied sickle cell anaemia and albinism at the molecular level.

Authorities claimed that the blogger died from complications due to sickle cell anaemia.

Sickle cell anaemia is a genetic disease.

A clear example of a mutation altering development is the inherited genetic defect, sickle cell anaemia.

The disease was named sickle cell anaemia in 1922 by Verne Mason after several additional cases were reported.

Children with sickle cell anaemia who are infected with Salmonella may develop osteomyelitis.

Sickle cell anaemia is an example.

There is still widespread ignorance about Sickle Cell Anaemia and the chances of passing it on.

A well-established case of heterozygote advantage is that of the gene involved in sickle cell anaemia.

People with sickle cell anaemia and thalassaemia are known to have red cells with defects in their outer membranes.

Susceptibility to bacterial infection is a hallmark of sickle cell anaemia, and a common cause of infant mortality.

The condition, which varies from mild forms to the most serious, Sickle Cell Anaemia, cannot be cured, but there is treatment.

As technology improves, adherents claim, we'll be able to engineer cures for hereditary diseases, from baldness to sickle cell anaemia.

Proceeds from the EP are to be donated to Sickle Cell Anaemia research.

A pioneering scheme to screen Afro-Caribbean people for the blood disorder Sickle Cell anaemia has been launched.

This type of anaemia is called haemolytic anaemia and is often caused by an inherited condition, such as sickle cell anaemia.

The Duffy antigen gene was the fourth gene associated with the resistance after the genes responsible for sickle cell anaemia, thalassemia and glucose-6-phosphate dehydrogenase.

For years, he had been prone to recurring attacks of Sickle Cell Anaemia, a rare and debilitating blood disorder that eventually triggered a premature heart attack.

January 30 - Workers from the National Institutes of Health announce the success of clinical trials testing the first preventative treatment for sickle cell anaemia.

The first report of sickle cell anaemia may have been in a report in 1846 where the autopsy report of an executed runaway slave was discussed.

Duffy antigen-negative individuals with sickle cell anaemia tend to suffer from more severe organ damage than do those with the Duffy antigen.

Symptoms of sickle cell anaemia are seldom manifest before the age of six months when the level of circulating fetal haemoglobin falls to the adult level.

During March of this year 5 of these patients all with homozygous sickle cell anaemia were admitted with aplastic crisis associated with parvovirus B19 infection.

A simple blood test can show whether a person has sickle cell disease.

In the case of sickle cell disease, both factors are often present.

Education for the public and professionals about sickle cell disease.

The most well known condition in this group is sickle cell disease.

Most states test for sickle cell disease before infants go home from the hospital.

Managing pain is often a big part of having sickle cell disease.

What can I do to manage the pain from sickle cell disease?

Sickle cell disease, which is most common in people of African descent.

This might happen if you are pregnant or have some medical problems, such as sickle cell disease.

"This is probably as good a mouse model you could ever have for sickle cell disease."

People with sickle cell disease and their families face ongoing stress.

"This means we should be able to make a major impact on stroke in children with sickle cell disease."

But the research efforts are now pointing to ways that could attack sickle cell disease directly.

Painful events are the most common symptom of sickle cell disease.

Home treatment for sickle cell disease includes steps you can take to control pain symptoms.

Eligibility: Children ages 3 to 19 with sickle cell disease.

People with sickle cell disease can appear pale or washed out.

Some complications of sickle cell disease may not need immediate medical attention from a doctor.

They also did important research on sickle cell disease.

For instance, isn't sickle cell disease much more common in blacks than whites?

Sickle cell disease is one of the most understood genetic diseases.

Children are born with sickle cell disease; it is not contagious.

Patients with sickle cell disease need ongoing treatment, even when they are not having a painful crisis.

Twenty years ago, children with sickle cell disease rarely lived to become adults.

He had no evidence of sickle cell disease or any other congenital blood disorders.

What are the different types of sickle cell disorders?

If your local community doesn't offer this option, look for a doctor and a pain treatment specialist who have experience in treating sickle cell disorders.

Depending on the other type of abnormal hemoglobin, these people may have mild or severe sickle cell disorder.

Hemoglobin D. This type of hemoglobin is present in a sickle cell disorder.

Persons with sickle cell disorders may suffer sickle cell crisis after receiving Neupogen.

A variety of sickle cell disorders result from inheritance of the sickle cell gene in a compound heterozygous manner with other mutant beta globin genes.

Severe sickle cell crises, in some cases resulting in death, have been associated with the use of NEUPOGEN in patients with sickle cell disorders.

Only physicians qualified by specialized training or experience in the treatment of patients with sickle cell disorders should prescribe Neupogen for such patients, and only after careful consideration of the potential risks and benefits.

Since then, Guthrie card samples have been collected routinely from infants in over 20 countries to screen for phenylketonuria and more recently for congenital hypothyroidism, sickle cell disorders and HIV infection.

Before using filgrastim, tell your doctor if you have sickle cell disorder, a blood cell disorder, chronic myeloid leukemia, myelodysplasia (also called "preleukemia"), or if you are receiving chemotherapy or radiation treatment.

Sickle cell syndromes.

"Or even mutating a gene to outsmart a local parasitic disease, like sickle cell syndrome to prevent malarial [46] infection," McCoy added.