Sickle Sentence Examples

A sickle, toothed like a saw, is used for reaping.

An old sickle mower and rake with their high metal seats were the only items she recognized.

Sickle cell anemia, also called sickle cell disease (SS disease), is an inherited condition caused by having abnormal hemoglobin, the protein that carries oxygen in the blood.

The increased risk among African Americans is not explained by the presence of sickle cell disease, nor is the excess risk among boys explained by trauma.

Sickle cell anemia-An inherited disorder in which red blood cells contain an abnormal form of hemoglobin, a protein that carries oxygen.

Sickle cell anemia does not predispose newborn infants to jaundice.

People with sickle cell anaemia have sickle hemoglobin (HbS) which is different from the normal hemoglobin (HbA).

Children with sickle cell anemia produce two abnormal hemoglobin proteins (inheriting one from each parent), which makes their red blood cells easily destructible while giving them a sickle-like shape.

By 1997, approximately 800 different diagnostic tests were available, most of them for hereditary genetic disorders such as Tay-Sachs disease, sickle cell anemia, hemophilia, muscular dystrophy, and cystic fibrosis.

Examples of genetic conditions include Down syndrome, Tay-Sach's disease, sickle cell disease, and hemophilia.

Severe diseases in the liver or kidneys, certain infections, sickle cell anemia, and some cancers also affect gonads.

Depending on your genetic background, you and your partner may also want to have a pregnancy blood test for genetic problems such as sickle cell disease or Tay-Sachs.

Blood donations benefit premature babies, cancer patients, individuals with sickle cell anemia and individuals undergoing surgery.

If you come from Russia the sickle and hammer paired with the bear could be your sign of patriotism.

The most common causes of stroke are congenital (present at birth) and acquired heart diseases, and sickle cell anemia.

About 10-15 percent of children with sickle cell disease suffer a stroke, usually ischemic stroke.

Sickle cell disease is a blood disorder in which the blood cells cannot carry oxygen to the brain because the blood vessels to the brain are either narrowed or closed.

Blood transfusions may be used to treat children with sickle cell disease.

Although there is a high risk of repeat strokes in patients with sickle cell anemia, the risk can be reduced with regular blood transfusions.

In addition, there is a blood test for fifth disease, but it is generally used only for pregnant women and for people who have weakened immune systems or who suffer from blood disorders, such as sickle cell anemia.

Sickle cell anemia is usually inherited from parents who are carriers, who have the sickle cell trait-a milder form of sickle cell anemia, or one abnormal hemoglobin.

Sickle cell anemia and sickle cell trait are found mainly in people whose families come from Africa, the Caribbean, the Eastern Mediterranean, Middle East, and Asia.

In the United States, sickle cell anemia affects some 72,000 people.

Some 2 million Americans carry the sickle cell trait and about one in 12 African Americans have the trait.

Sickle cell anemia is caused by an error in the gene that signals the body how to make hemoglobin.

Children suffering from sickle anemia have episodes during which they suddenly become unwell or complain of severe abdominal or chest pain, headache, stiffness of the neck or drowsiness.

Parents should know that a child having a sickle cell crisis requires urgent hospital treatment.

The diagnosis of sickle cell anemia is established during the newborn screen testing that is performed in the nursery at time of birth.

For children who are not tested, an electrophoresis test of the blood can detect the abnormal hemoglobin of sickle cell anemia.

Children with sickle cell disorders are at risk of developing severe infections, and penicillin is usually prescribed to prevent dangerous pneumococcal infections.

Bone marrow transplantation has been shown to provide a cure for severely affected children with sickle cell disease, but the procedure is not entirely without risk.

In addition, the marrow must come from a healthy matched sibling donor and only about 18 percent of children with sickle cell anemia are likely to have a matched sibling.

Research contributed a great deal about sickle cell anemia from 1970 to the early 2000s concerning what causes it, how it affects the patient, and how to treat it.

Scientists were as of 2004 starting to be successful at developing drugs that prevent the symptoms of sickle cell anemia and procedures that they hope should eventually provide a cure.

It has been observed that some children with sickle cell anemia continue to produce large amounts of fetal hemoglobin after birth, and studies have shown that these children have less severe cases of the disease.

Thirst and dehydration caused by not drinking enough, even if thirst is not felt, are known to trigger sickle pain.

Children with sickle cell anemia are anemic to various degrees.

Both sickle cell trait and sickle cell anemia are inherited.

If one partner has sickle cell trait and the other does not, their children each have a 50 percent chance of having the sickle cell trait, and a 50 percent chance of having normal hemoglobin.

If one parent has sickle cell trait it is extremely important that the other parent be tested.

If both parents have sickle cell trait and want to know whether the unborn child has sickle cell anemia, testing can be performed as early as the tenth week of pregnancy.

Parents should be aware that children with sickle cell anemia are also at increased risk of infection, especially from the Streptococcus pneumonia and H. influenzae bacteria.

Sickle cell anemia does not affect intelligence.

Children with sickle cell disorders can almost always attend school and participate fully in normal activities.

Sickle cell trait-Condition that occurs in people who have one of two possible genes responsible for the abnormal hemoglobin of sickle cell anemia.

People with this trait may suffer milder symptoms of sickle cell anemia or may have no symptoms.

J., et al. "Declining stroke rates in Californian children with sickle cell disease."

H. "Therapies to increase fetal hemoglobin in sickle cell disease."

A., et al. "Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease."

Children older than five years do not need vaccination, unless the child or adolescent has a serious health problem that lowers immunity, such as HIV infection, sickle cell disease, or is being treated for cancer.

Sickle cell anemia is an inherited, chronic, incurable blood disorder that causes the body to produce defective hemoglobin, the abnormal HgbS, which occurs primarily in African Americans.

Unlike normal oval cells, fragile sickle cells cannot hold enough hemoglobin to nourish body tissues.

The deformed shape makes it hard for sickle cells to pass through narrow blood vessels.

When capillaries become obstructed, a life-threatening condition called sickle cell crisis is likely to occur.

A child who inherits the sickle cell gene from each parent will have the disease.

A child who inherits the sickle cell gene from only one parent carries the sickle cell trait but does not have the disease.

Sickle cell anemia is more frequently diagnosed than thalassemias and occurs most often among African Americans.

Diagnosing thalassemia and sickle cell anemia, both of which involve disorders of hemoglobin, will require measuring the different types of hemoglobin through a laboratory testing method called hemoglobin electrophoresis.

Sickle cell anemia will be monitored by regular eye examinations and diagnostic blood work.

Immunizations for pneumonia and infectious diseases are part of treatment along with prompt treatment for sickle cell crises and infections of any kind.

The hereditary anemias, such as the thalassemias and sickle cell anemia, may require life-long treatment and monitoring whereas other types of anemia, once treated, are apt not to recur.

Managing Sickle Cell Disease in Low-Income Families.

Fetal hemoglobin measurement helps diagnose a group of inherited disorders that affect hemoglobin production, among which are the thalassemias and sickle cell anemia.

For example, HbF can be found in higher levels in sickle cell anemia and other hereditary anemias.

Sickle cell anemia, the inherited condition characterized by curved (sickle-shaped) red blood cells and chronic hemolytic anemia, is an example of the first category.

Cade joined her and climbed up into the seat on the sickle.

Earth excited Cronus to attack the father, whom he castrated with a sickle.

Individuals with sickle cell trait, although generally asymptomatic, can develop symptoms of sickling if exposed to very low oxygen pressures.

Patients with sickle cell disease are treated at The Royal London.

Objectives To assess the effects of routine malaria chemoprophylaxis in people with sickle cell disease.

People with Sickle Cell Anemia often have mild jaundice which can make the whites of their eyes look yellowish.

Many people are familiar with the fact that the old Druids harvested mistletoe from the Oak with a golden sickle.

To achieve the lowest possible childhood death rate and to minimize childhood morbidity from sickle cell disorders.

On its highest pinnacle floated a large red flag with a yellow sickle and hammer in one corner.

Within his bending sickle 's compass come; which alters when it alteration finds, it is the star to every wand'ring bark.

Climb across using a large sickle shaped layaway to gain a small hold continue to the break.

And another angel came out of the temple in heaven, and he too had a sharp sickle.

The Welsh dragon on the left carries a sickle to represent farming interests.

In one corner is the head of a woman wearing a radiant crown, a goddess, holding a sickle.

The tall sickle shaped fin is situated well back on the blackish body and the blow is rarely seen.

Carriers of sickle Cell are sometimes said to have ' sickle cell trait ' .

Gaia made a flint sickle and invited Kronos and his brothers to kill Uranus.

But instead of the black swastika in the middle is a black hammer and sickle.

To the right and high up in the sky was the sickle of the waning moon and opposite to it hung that bright comet which was connected in Pierre's heart with his love.

In her office she hung a red flag with a hammer and sickle on it.

Plain English Summary Antenatal screening for haemoglobinopathies (thalassaemia and sickle cell disease) has been available since the 1970s.

A sickle shaped implement with an angled blade for close cutting.

So he who sat upon the cloud swung his sickle on the earth, and the earth was reaped.

Carriers of Sickle Cell are sometimes said to have ' sickle cell trait '.

If an individual inherits one sickle hemoglobin gene they generally have no symptoms but they can pass this gene on to their children.

Back to top Why might I be tested for sickle cell anemia?

Sickle cell anemia is an inherited disease and lasts a lifetime.

You use this lever to lower the sickle, like this and then lift it over stumps and such.

In her right hand she holds her golden sickle.

These waters had been erroneously taken for parts of one vast horseshoe or sickle shaped lake, only some 20 m.

The young crop was hoed, reaping was performed with a sickle, and a high stubble left on the ground as manure.

In shape it is not unlike the sickle (drepane), to which it was compared by the ancients,--the hollow side, with the town and harbour of Corfu in the centre, being turned towards the Albanian coast.

Some Finnish geologists - Sederholm for one - consider it probable that during the Glacial period an Arctic sea (Yoldia sea) covered all southern Finland and also Scania (Sickle) in Sweden, thus connecting the Atlantic Ocean with the Baltic and the White Sea by a broad channel; but no fossils from that sea have been found anywhere in Finland.

Reckon seven weeks from the time of putting the sickle to the standing corn.

They radiate from a point within the Sickle of Leo and are termed Leonids.

South of a line running, roughly, from the foot of Lake Vener to Kalmar on the Baltic coast the beech begins to appear, and in Sickle and the southern part of the Cattegat seaboard becomes predominant in the woods which break the wide cultivated places.

The suggestion that the eating of cakes of unleavened bread, similar to the Australian "damper," was due to the exigencies of the harvest does not meet the case, since it does not explain the seven days and is incongruous with the fact that the first sheaf of the harvest was put to the sickle not earlier than the third day of the feast.

The sickle was of wood (92), with flints (91) inserted, apparently a copy of the ox-jaw and teeth.