Through HPLC (High performance liquid chromatography) test one can know the presence or absence of haemoglobin S .
A pretest before child birth is also a useful one.
diagnosis of the amniotic sac is a very useful .
Yes, an adult can be diagnosed with sickle cell anemia. The condition is usually detected in childhood through newborn screening or during genetic testing later in life. Adults who have not been previously diagnosed may present with symptoms such as anemia, pain crises, or complications related to sickle cell disease.
A child has to receive the gene from both parents to heve sickle cell anemia. if only one parent passes on the gene, then the child will have sickle cell trait, but no symptoms of sickle cell anemia.
Spherocytosis
Hemoglobin SS disease (Hb SS)
People who inherit one sickle cell gene are said to have sickle cell trait. This means they carry the gene but do not typically have symptoms of sickle cell disease. It is important for individuals with sickle cell trait to be aware of their status for proper medical management and genetic counseling.
Sickle cell is diagnosed by a simple blood test called hemoglobin electrophoresis. This analyzes the blood and points out abnormal cells.
Sickle Cell....... My son has been diagnosed with sickle cell trait. We are white and the doctors called it Sickle Cell Trait! hope this helps...
T- Boz
yes because anyone can get that disease
When you have been diagnosed with it by a medical doctor by lab testing.
Yes! sickle cell can be tested prenatally. Such testing can even be done before the zygote develops into a foetus thus making it possible for a potentially sickle cell diseased foetus to be aborted or even genetic manipulations to be carried to repair the mutation and the zygote reintroduced into the mother to develop.
Yes, an adult can be diagnosed with sickle cell anemia. The condition is usually detected in childhood through newborn screening or during genetic testing later in life. Adults who have not been previously diagnosed may present with symptoms such as anemia, pain crises, or complications related to sickle cell disease.
A sample of blood is looked at under a microscope. The sickled cells are then seen.
a person who receiver traits from anothr karyotype
What is sickle cell disease?Sickle cell disease is an inherited disorder that affects red blood cells. People with sickle cell disease have red blood cells that become hard and pointed instead of soft and round. Sickle cells cause anemia, pain and many other problems.Top2) What is sickle cell trait?If you have sickle cell trait, you have inherited the gene for sickle cell disease. Sickle cell trait does not turn into sickle cell disease. If someone has sickle cell trait and his partner has sickle cell trait they may produce a child with sickle cell disease. There are about 2.5 million people in America with sickle cell trait.Top3) If sickle cell trait is not an illness, why are people tested?Babies are tested to see if they have sickle cell disease. Teens and adults are tested mainly to see if they can have a baby with the disease.Top4) What medical problems are caused by sickle cell disease?Lung tissue damage, pain episodes and stroke. The blockage of blood flow caused by sickled cells also causes damage to most organs including the spleen, kidneys and liver.Top5) How many people have sickle cell disease?Sickle cell disease is a global health problem. In the United States it is estimated that over 70,000 people have sickle cell disease. About 1,000 babies are born with the disease each year in America.Top6) How long does a person with sickle cell disease live?The average life expectancy in America has improved. It is now in the mid 40 years of age range.Top7) Are people of African descent the only group affected?No. It is also present in Portuguese, Spanish, French Corsicans, Sardinians, Sicilians, mainland Italians, Greeks, Turks and Cypriots. Sickle cell disease also appears in Middle Eastern countries and Asia.Top8) Is there a cure?There is no universal cure for sickle cell disease. Research in gene therapy, the ultimate universal cure, is currently underway.Top9) What are some promising treatment developments?The use of hydroxyurea has shown promising results on some adult sickle cell patients. It reduces the frequency of severe pain, acute chest syndrome and the need for blood transfusions.Top10) Can people with sickle cell disease live a productive life?Yes. But like all patients with chronic disease, sickle cell patients are best managed in a comprehensive multi-disciplinary program of care and a strong extended support system.
No. Not all children will have it. Only those of African decent.
Sickle cell disease is a genetic condition that a child inherits from their parents, and symptoms typically manifest in early childhood. A child cannot "get" sickle cell disease at the age of sixteen if they do not already have the genetic traits for it. However, if a person has the sickle cell trait, they may not show symptoms until later in life, but the underlying genetic condition is present from birth. Therefore, a child diagnosed with sickle cell disease at sixteen would have had it since birth, but symptoms may not have appeared until later.