Basic Sciences Flashcards
Pituitary microadenomas are smaller than_____ mm in diameter.
10
What is Sutherland’s classification for nerve injury?
- 1st degree Reversible conduction block.
- 2nd degree Wallerian degeneration occurs but endoneurium stays intact and recovery is usually complete.
- 3rd degree Endoneurium is destroyed but perineurium stays intact and recovery is incomplete.
- 4th degree All is destroyed except for the epineurium; recovery is poor.
- 5th degree Complete nerve transection; untreated recovery is not expected.
When during the day does growth hormone production peak?
2-3 hours into sleep (stage III or IV).
How long does it take for Wallerian degeneration to occur after complete nerve transaction?
3 days
What is the half-life ofT4?
7 days.
Which part of the pituitary gland is derived from Rathke’s pouch?
Anterior pituitary.
In patients treated for thyroid cancer, posttherapy thyroglobulin levels are less useful in the presence of elevated’—_.
Antithyroglobulin antibodies.
What structures facilitate passage of CSF into the dural venous sinuses?
Arachnoid villi.
Which of these result in Wallerian degeneration?
Axonotmesis and neurotmesis.
What hormone is produced by the parafollicular C cells of the thyroid?
Calcitonin.
What are the three primary ways a cell reacts to a hormonal signal?
Changing its metabolite or protein; generating an electric current; contracting.
What produces CSF?
Choroid plexus.
The parasympathetic nervous system originates in the segntents of the spinal cord while the sympathetic nervous system originates in the segntents of the spinal cord.
Craniosacral; thoracolumbar.
Secretion of ADH from the posterior pituitary gland results in decreased or increased urine volume?
Decreased.
Secretion of TSH from the anterior pituitary gland results in increased or decreased colloid production in the thyroid gland?
Decreased.
What hormone receptors are present in juvenile nasopharyngeal angiomas?
Dihydrotestosterone and testosterone.
What time of day does cortisol production peak?
Early morning.
How many cervical spinal nerves are there?
Eight.
Which thyroid blood test correlates best with the metabolic state of the patient?
Free thyroxine index (FT41).
When is clock-dependent alerting most active?
In the afternoon.
What effect does PTH have on urine phosphorus?
Increases urine phosphorus excretion.
Which hormone normally regulates protein synthesis and breakdown?
Insulin.
What is “clock-dependent alerting”?
Internal signal from the biological clock that opposes the tendency to fall asleep.
What are the two major classes of hormone receptors?
Membrane receptors, binding peptides and catecholamines, and nuclear receptors, binding small molecules that can diffuse across a cell membrane.
What are the three types of nerve injury?
Neuropraxia, axonotmesis, and neurotmesis.
Which of these has a more rapid rate ofWallerian degeneration?
Neurotmesis.
Steroid hormones and thyroid hormones use which type of receptor?
Nuclear.
What will happen to reverse T3 and T3 levels during fasting, systemic illness, and acute psychiatric illness?
Reverse T3 levels will increase and T3 levels will decrease.
What happens to PTH levels as people age?
Rise.
What is the most common cause of diabetes insipidus?
so% of cases are idiopathic.
What is the major inhibiting hormone to growth hormone?
Somatostatin.
What effect do exercise and stress have on growth hormone secretion?
Stimulate secretion.
Where in the brain is the “biological clock”?
Suprachiasmatic nuclei.
What is the major inhibiting hormone ofTSH?
T3.
Which of these sends motor and sensory fibers to the posterior and superior scalp as the greater occipital nerve?
The second cervical nerve.
The thyroid hormones are stored as , the main component of colloid.
Thyroglobulin.
The FT41is the product of total T4 level and what?
Thyroid hormone binding ratio (THBR).
Most of the circulating thyroid hormone is bound by.
Thyroxine-binding globulin.
Motor impulses are carried by the root of the spinal cord and sensory impulses are carried by the root of the spinal cord.
Ventral; dorsal.
What substance is unique to CSF, perilymph, and vitreous humor?
β-2-transferrin
What is a Type I error?
A false-positive result.
A prospective cohort study where exposure to the risk factor and subsequent health outcomes are observed after the beginning of the study is also known as what?
A longitudinal study.
Observational studies where the subjects are sampled based on presence or absence of disease and then their prior exposure status is determined are known as what?
Case-control studies.
Observational studies where the investigator determines the exposure status of the subjects and then follows them for subsequent outcomes are known as what?
Cohort studies.
What happens to the required sample size if the variability of the outcome diminishes?
Decreases.
How is the required sample size affected if one decreases the acceptable type I error?
Increases.
What are the advantages of case-control studies over cohort studies?
Less expensive and time-consuming and easier for studying rare diseases.
Tests with high sensitivity are useful to rule in or rule out disease?
Rule out.
What are the three primary forms of bias?
Selection bias, information bias, and confounding.
What is external validity?
The extent to which the results of a study are applicable to other populations.
What is the beta level of a test?
The likelihood of obtaining a type II error (false-negative).
1 - beta= _____
The statistical power (likelihood of detecting a true difference between the groups).
In autosomal recessive disorders, what is the risk of a child receiving a mutant gene from both parents and having the recessive trait?
25%.
What is the risk of the sibilings of affected persons being carriers?
67%.
What does 47, XY+21mean?
A male with three copies of chromosome 21.
What is genetic anticipation?
A phenomenon seen in disorders caused by unstable trinucleotide repeats where the age of onset of the disorder is younger and the phenotype becomes more severe with each succeeding generation.
How could a person with an autosomal dominant disease have no affected family members?
Due to a new mutation in the gene or nonpenetrance, where the gene lacks a phenotypic effect in a known carrier.
Autosomal recessive conditions are frequently associated with. defects whereas autsosomal dominant conditions are frequently associated with defects.
Enzyme; protein structure.
True/False: All complete autosomal monosomies are lethal early in development.
False; sex chromosome monosomy, such as Turner syndrome (45,X), can be viable.
What is an association?
Malformations occurring together more frequently than would be expected from chance alone.
What is the term for cell division in gametes?
Meiosis.
In which type of genetic defect can the father not pass a mutation to any offspring?
Mitochondrial defects.
What is a sequence?
Multiple defects arising from a single structural anomaly where the order of maldevelopment is understood.
What is a syndrome?
Pattern of multiple anomalies pathogenetically related.
Which type of inheritance pattern has a recurrence risk that varies with the number of affected family members?
Polygenic inheritance.
A classic example of genetic imprinting is seen with microdeletions of the region 15q11to 15q13. A microdeletion of the paternal chromosome 15 causes and microdeletion of the maternal chromosome 15 causes.
Prader-Willi syndrome; Angelman syndrome.
What syndrome is caused by a microdeletion in chromosome 17 and is associated with mental retardation, broad feet and hands, peripheral neuropathy, hearing loss and recurrent otitis media, disturbed sleep patterns, and inserting foreign objects into bodily orifices?
Smith-Magenis syndrome.
What is mosaicism?
The presence of two or more different chromosome constitutions in different cells in the same individual (i.e., may have some cells with 46 chromosomes and some with
Hurler-Scheie syndrome is caused by which gene mutations with which inheritance pattern?
This syndrome is inherited in an autosomal recessive pattern with the phenotype a product of two different mutations of the IDUA gene (compound heterozygotes.)
What are the most common numerical chromosome abnormalities in humans?
Trisomies.
What is a microdeletion syndrome?
Variable phenotypic pattern resulting from duplication or deletion of a small segment of linked chromosome material/genes that are functionally unrelated.
What is the concentration of immunoglobulins in the perilymph compared to the serum?
1/1000th.
What is the mechanism of type IV or delayed-type hypersensitivity immune reactions?
An overenthusiastic T-cell response to an environmental antigen where macrophages damage adjacent tissues.
What type ofT-cell receptor do Class II MHC antigens have?
CD4