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Thalassemia : is an inherited blood disorder characterized by less hemoglobin and fewer red blood cells in your body than normal.
Monogenic : controlled or involving a single gene.
Fixation : a term in population genetics denoting that a mutant allele for a particular gene has become the only allele expressed in the population.
Epidemiology : the branch of medicine that deals with the incidence, distribution, and possible control of diseases and other factors relating to health.
Hemoglobinopathies : Is a genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin molecule.
Hemolytic anemia : when red blood cells die sooner than the bone marrow can produce them.
Asymptomatic : producing or showing no symptoms.
Hypoxia : Depravation of oxygen in the entire body or specific regions.
Preeclampsia : a condition in pregnancy characterized by high blood pressure, sometimes with fluid retention and proteinuria.
Polyhydramnios : is a medical condition describing an excess of amniotic fluid in the amniotic sac
Splenomegaly : abnormally enlargement of the spleen
Splenectomy : a surgical operation involving the removal of the spleen
Hydrops fetalis : accumulation of fluid in the fetus.
Prenatal : before birth, related or during pregnancy.
Hematologic : is the study of blood in health and disease
Heterogeneity : is a word that signifies diversity.
Microcytocis anemia : is any type of anemia characterized by unusually small red blood cells.
Phenylketonuria : an inherited inability to metabolize phenylalanine that causes brain and nerve damage if untreated.
Homozygous : Individual that has two copies of the same allele aa
Heterozygous : Individual has two different copies of the same allele Aa
- is an inherited blood disorder characterized by less hemoglobin and fewer red blood cells in your body than normal.
- controlled or involving a single gene.
- a term in population genetics denoting that a mutant allele for a particular gene has become the only allele expressed in the population.
- the branch of medicine that deals with the incidence, distribution, and possible control of diseases and other factors relating to health.
- Is a genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin molecule.
- when red blood cells die sooner than the bone marrow can produce them.
- producing or showing no symptoms.
| - Depravation of oxygen in the entire body or specific regions.
- a condition in pregnancy characterized by high blood pressure, sometimes with fluid retention and proteinuria.
- is a medical condition describing an excess of amniotic fluid in the amniotic sac
- abnormally enlargement of the spleen
- a surgical operation involving the removal of the spleen
- accumulation of fluid in the fetus.
- before birth, related or during pregnancy.
| - is the study of blood in health and disease
- is a word that signifies diversity.
- is any type of anemia characterized by unusually small red blood cells.
- an inherited inability to metabolize phenylalanine that causes brain and nerve damage if untreated.
- Individual that has two copies of the same allele aa
- Individual has two different copies of the same allele Aa
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PuzzleFast.com, Noncommercial Use Only
- THALASSEMIA
- MONOGENIC
- FIXATION
- EPIDEMIOLOGY
- HEMOGLOBINOPATHIES
- HEMOLYTICANEMIA
- ASYMPTOMATIC
| - HYPOXIA
- PREECLAMPSIA
- POLYHYDRAMNIOS
- SPLENOMEGALY
- SPLENECTOMY
- HYDROPSFETALIS
- PRENATAL
| - HEMATOLOGIC
- HETEROGENEITY
- MICROCYTOCISANEMIA
- PHENYLKETONURIA
- HOMOZYGOUS
- HETEROZYGOUS
|
© 2015
PuzzleFast.com, Noncommercial Use Only