Exam 1 Flashcards
coagulative necrosis with impaired bloodflow and bacterial invasion
Gangrene
enzyme dissolve and liquefy necrotic cells
liquefaction necrosis
necrotic debris remain
caseous necrosis
lipase enzyme break down intracellular triglyceride to fat
fat necrosis
interruption of blood flow
coagulative necrosis
dry brown/black skin with minimal bacterial infection
dry gangrene
with liquefaction necrosis dmg from bacteria and white blood cell produce wound
wet gangrene
presence of Clostridium
gas gangrene
tumor, cell growth not responding to normal regulator process.
neoplasm
uncontrolled growth
cancer
loss of differentiation occurring with cancer
anaplasia
less anaplastic tumor cells producing rapidly but cause fewer problems
benign
spread
metastasize
anaplastic, nonfunctioning cells reproducing rapidly
malignant
eradicate disease
treat or increase comfort
prevent disease
curative
palliative
prophylactic
likelihood of surviving cancer
prognosis
cancer responded to treatment and is under control
remission
study of heredity
genetics
birth defects
congenital defects
cellular instruction and information carried in
genes
template of protein synthesis
DNA
double stranded chain of nucleotide
chromosome
22 set paired chromosomes
autosomes
representation of individual chromosome
karyotype
physical expression of gene
phenotype
absence of diploid (normal chromosome)
most common is down’s syndrome
autosomal aneuploid
single gene mutation passed from affected parent to offspring
autosomal dominant
gene that has many variation
allele
single gene mutation passed from affect parent to offspring only in homozygous allele pair
autosomal recessive
euploid cell has more than diploid number of chromosome
polypoidy
3 chromosome XXY
testicle fail to mature
gyno
sexual dysfunction
klinefelter’s syndrome
only one XY chromosome due to deletion of part or al of chromosome
short
lymphedema of hand and feet
turner’s syndrome
percentage of individual with genotype and also express phenotype
penetrance
extent of variation in phenotype associated with genotype
expression
deficiency of enzyme phenylalanine for conversion to tyrosine due to mutation on chromosome 12
failure to meet milestone
microcephaly
seizure
hyperactive
PKU
deficiency of hexosaminidase, lysosomal enzyme necessary to metabolize lipids and destroy nerve cells
vision, hearing, loss
paralysis
seizures
taysach’s
neurogenic tumor from schwann cells
Type 1: raised lumps
type 2: tumor cause hearing loss
neurofibromatosis
gene located on x (sex) chromosome
single recessive copy effect male
2 required for female
sex linked
x-linked dominant disorder, failure to express protein for neural development
intellectual, learning disability
prominant jaw and forhead
fragile x syndrome