Ch. 2 Test Flashcards
Muscular distrophy
Group of genetic diseases marked by progressive weakness of skeletal muscle fibers
Sickle cell anemia
Misshapen cells produce abnormal hemoglobin in the RBC’s
Cystic fibrosis
Disorder of the exocrine glands
Tray-sachs disease
Marked by varying degrees of mental retardation and physical abnormalities
Phenylketonuria
Essential digestive enzyme is missing; may be detected by blood test at birth; if undetected or untreated mental retardation occurs
A hereditary disease
Disease marked by progressive physical degeneration, mental retardation and early death
Hemophilia
Hereditary bleeding disorder caused by a missing blood clotting factor. Passed from mother to son
Huntingtons disease
Signs and symptoms appear midlife; there is irreversible and progressive loss of muscle control and mental ability. Caused by dominant gene
Nosocomial infection
Hospital acquired infection. Was not present at admission but appeared 72+ hrs. After admission
Idiopathic
Disease with no known cause
Iatrogenic
Disease caused by the doctor or as part of the treatment
Organic disorder
Pathological physical changes that explain a patients signs and symptoms
Functional disorder
No pathological physical changes to explain the patients signs and symptoms
Mesentary
Layer of peritoneum that suspends part of the intestines within the abdominal cavity
Anomaly
Any deviation from what is regarded as normal
Where embryonic cells are found and why Theyre valuable
Found in the cord blood from the umbilical cord and placenta of newborn infants
How many chromosomes are in most cells? Gamete cells?
23 pairs and 23 single cells
Congenital
Present at birth
Gerontologist
A physician that specializes in care of old people
Cerebral palsy
Result of brain damage andnis a congenital condition caused by birth injury
Physiology
Study of the functions of the body (how it works)
Anatomy
Study of the structures of the body(what it looks like)