An abnormal chromosome analysis report will include the total number of chromosomes and will identify the abnormality found. Tests for gene mutations will report the mutations found.
the homeophrangular mocecule
A genetic blood test can reveal the existence of certain substances in people who have a tendency to develop narcolepsy. Positive test results suggest narcolepsy.
The genetic traits, both physical and behavioral, that the individual possesses on his personal genome.
1. (1) Produced by an abnormality in, or a mutation of the genetic code in a single gene; (2) Caused by several abnormal genes (Producing so-called polygenic diseases); or (3) Caused by the abnormal presence or absence of an entire chromosome or by alteration in the structure of chromosomes.
Practically every genetic disorder that includes physical characteristics affects facial features. The term is dysmorphic facial features genetic disorders.
Greater than 2% of total hemoglobin is abnormal.
Abnormal findings in the basal gastric secretion test are considered nonspecific and must be evaluated in conjunction with the results of a gastric acid stimulation test. Elevated secretion may suggest different types of ulcers.
Yes, a hydatidiform mole is due to genetic abnormalities that result in the abnormal development of the placenta. It occurs when there is an abnormal fertilization of an egg by a sperm, leading to an abnormal growth of tissue in the uterus.
It is a genetic syndrome characterized by abnormal movements.
Abnormal crystals and amorphous sediment are findings in a urine test, not a blood test. Suggests stones.
An abnormal condition that a person inherits through the chromosomes or genes is a genetic disorder.
urinalysis is a very common diagnostic test . describe and name the possible abnormal results related to this test. indicate the disorders that these abnormal results may suggest.
GES scan studies that show emptying of the stomach in a longer than accepted period is abnormal. Severity of test results and symptoms do not always match; therefore, the physician must carefully interpret these findings. Diabetic.
If the multiple of the median value is above 2.0 MOM or 2.5 MOM (depending on the laboratory), the fetus is considered to be at a higher risk for a genetic defect.
An obvious increase in strength in weakened muscles strongly suggests the diagnosis of myasthenia gravis. The effect comes on very rapidly, and fades within minutes.
A diseased external sphincter muscle will produce an abnormal pattern of electrical activity.
genetic characteristics