Malaria and
sickle cell samples were obtained from patients confirmed to have each disease.
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 trait.
The tenth week is usually the time that a chorionic villus
sampling (CVS) is performed, which will check for genetic abnormalities like
sickle cell anemia, Down Syndrome, cystic fibrosis and Tay - Sachs disease.
With a miniscule blood
sample, the HemeChip, a micro-electrophoretic device, examines and identifies hemoglobins, including hemoglobinopathies
sickle cell anemia (HbSS),
sickle trait (HbAS) and SC disease (HbSC).
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.
Toward this end we have built a mobile phone - mounted light microscope and demonstrated its potential for clinical use by imaging P. falciparum - infected and
sickle red blood
cells in brightfield and M. tuberculosis - infected sputum
samples in fluorescence with LED excitation.
In this high - tech lab, students can perform tests like gel electrophoresis, analyzing hemoglobin
samples to determine whether a patient has
sickle cell disease.
It has been used in
samples of children with cancer, diabetes, juvenile rheumatoid arthritis, and
sickle cell disease.