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137 Cards in this Set

  • Front
  • Back
Mineral deficiency characterized by alopecia, dermatitis, diarrhea
zinc
1g of alcohol equals how many kcal?
7kcal
Erlenmeyer flask shaped lesions in the long bones suggest what storage disorder
Gaucher's disease
enzyme deficiency in porphyria cutanea tarda
uroporphyrinogen decarboxylase
characterized by recurrent abdominal pain, photosensitivity, blistering of the skin in sunlight, and bizarre behavior
porphyria cutanea tarda
the MOST common porphyria
cutanea tarda
amenorrhea in Anorexia Nervosa is caused by what
decreased LH
symptoms of opioid toxicity
lethargy, obtundation, respiratory depression, pinpoint pupils
symtpoms of ethanol withdrawal
tachycardia, diaphoresis, agitation, confusion, disorientation
endogenous enzyme used to detoxify acetaminophen metabolites
glutathione
symptoms include proptosis, swellingof the eyeball, black discoloration of the nasal turbinates, anterior displacement of the eye, filling of the maxillary and ethmoid sinuses; increased risk of occuring in diabetics
rhinocerebral mucormycosis (nonseptate hyphae)
typical cause of AIDS lymphoma
epstein-barr virus
disease characterized by abnormal platelet adhesion
von Willebrand disease
clotting factor decreased in von Willebrand disease
VIII
dementia most common in boxers or football players (due to head trauma)
dementia pugilistica
Broadmann's areas for Broca's and Wernicke's areas
44 (Broca's) and 22 (Wernicke's)
disease characterized by lack of fluency, lack of comprehension, and impaired repetitive speech
Global aphasia
characterized by agraphia, acalculia, R-L disorientation, and finger agnosia
Gerstmann's syndrome
location of lesion causing Gerstmann's syndrome
dominant (L) inferior parietal lobule
MOST common side of hemineglect
L
characterized by simultanagnosia, optic taxia, ocular ataxia; caused by bilateral lesions of the dorsolateral parieto-occipital association cortex
Balint's syndrome
DOC for ADHD
methylphenidate
Form of vascular dementia characterized by diffuse subcortical infarcts associated with chronic HTN cause this form of dementia
Binswanger's disease
neurotransmitter(s) affected in Alzheimer's
Ach
3 types of vascular dementia
multi-infarct dementia, Binswanger's disease, cerebral amyloid angiopathy
treatment of Alzheimer's disease includes these drugs
rivastigmine, galantamine, donepezil, tacrine
class of drugs used to treat Alzheimer's disease
acetylcholinesterase inhibitors (AChE inhibitors)
anti-muscarinic used in Parkinsons
benzotropine
anti-muscarinic used in motion sickness
scopolamine
pralidoxime is used to treat what overdose
organophosphates
anti-muscarinic used to cause mydriasis and cycloplegia
cyclopentolate
2 key structures of the medial temporal lobe
hippocampal formation and parahippocampal gyrus
function of medial temporal lobe and medial diencephalic areas
memory
cortex of the parahippocampal gyrus which functions in smell and memory; its the main input to the hippocampal formation
entorhinal cortex
the perforant pathway of the hippocampal formation, granules cells, mossy fibers of CA3, and Schaffer collateral CA1 connections are all needed for what process
LTP
3 major nuclei of the amygdala
corticomedial, basolateral, and central nuclei
prevalence of epilepsy in the general population
1%
risk of having a single seizure in one's life
10-15%
what the difference between clonic and tonic movements
clonic involves rhythmic jerky movements, and tonic involves sustained (isometric) contractions
treatment of atypical depression (increased sleep)
MAOIs
DOC for OCD
clomipramine
anti-seizure drugs that block voltage-gated sodium channels
phenytoin, carbamazepine, lamotrigine (Na+ and Ca++), zonisamide
both phenobarbital and benzodiazepines (that are used as anti-epileptics) have a MOA as a GABA agonist... but how do their MOAs differ?
benzodiazepines increases the FREQUENCY of Cl- channel opening, and phenobarbital increases the DURATION of Cl- channel opening
anti-seizure drugs that block voltage-gated calcium channels
ethosuximide, gabapentin, lamotrigine (Na+ and Ca++)
anti-seizure drug that acts by opening K+ channels
valproic acid
DOC for tonic-clonic (grand mal) seizures
valproic acid, carbamazepine, phenytoin, lamotrigine, topiramate
DOC for partial seizures
carbamazepine, lamotrigine, phenytoin
DOC for absence seizures
clonazepam, ethosuximide, valproic acid
DOC for myoclonic seizures
valproic acid
DOC for status epilepticus
diazepam and lorazepam (short term), or phenytoin (long term)
DOC for status epilepticus in children
phenobarbital
class of drugs used when normal measures to treat status epilepticus fail
general anesthetics
DOC for trigeminal neuralgia
carbamazepine
anti-seizure drugs used in bipolar disorder
valproic acid, carbamazepine, lamotrigine
anti-seizure drug that can be used to help treat migraines
phenytoin and topiramate
anti-seizure drug that can treat pain of neuropathic origin
gabapentin
SE to the fetus when a pregnant mother takes anti-seizure medication
neural tube defects, craniofacial anomalies, and fetal hydantoin
life-threatening SEs that lamotrigine and carbamazepine both share
steven-johnson syndrome and toxic epidermal necrolysis
embryogenesis gene in the zone of polarizing activity that patterns along the AP axis
sonic hedgehog
embryogenesis gene produced at the apical ectodermal ridge that organizes along the dorsal-ventral axis
Wnt-7
embryogenesis gene produced at the apical ectodermal ridge that stimulates mitosis
FGF
embryogenesis gene involved in segmental organization of the embryo in a craniocaudal direction
homeobox
what week does the bilaminar disk form
week 2
2 layers that make up the bilaminar disk
epiblast and hypoblast
what week does gastrulation, primitive streak formation, notochord development, and neural plate formation occur
week 3
when does the neural tube close
week 4
when does the heart begin to beat
around day 21 (week 4 according to first aid)
when do limb buds form
week 4
when can you differentiate between male and female in the fetus
week 10
what plate control sensory development
alar plate (dorsal)
what plate controls motor development
basal plate (ventral)
what does the notochord become in the adult
nucleus propolsus
the adenohypophysis (Rathke's pouch), lens of the eye, lining of the oral cavity, sensory organs of the ear, olfactory epithelium, epidermis, and the glands form from what part of the ectoderm
surface ectoderm
the brain, retina, and spinal cord for from what part of the ectoderm
neuroectoderm
the dorsal root ganglia, cranial nerves, melanocytes, chromaffin cells, C cells, Schwann cells, meninges, skull bones form from what part of the ectoderm
neural crest
when is a fetus MOST susceptible to teratogens in the mother
organogenesis period (weeks 3-8)
what teratogen is the leading cause of birth defects and mental retardation in the fetus
alcohol
teratogen causing CN VIII toxicity
aminoglycosides
teratogen causing placental abruption
cocaine
teratogen causing clear cell adenocarcinoma
DES
teratogen causing Ebstein's anomaly
lithium
teratogen that is the most common cause of preterm labor and IUGR
smoking
teratogen associated with discolored teeth in the fetus
tetracyclines
teratogen (overdose) leading to an EXTREMELY high risk of spontaneous abortion
vitamin A toxicity
teratogen that increases risk of neural tube defects even in mothers taking adequate folate
valproate
characterized by retardation, microcephaly, holoprosencephaly, marked facies ("seal face"), limb discoloration, and heart/lung fistulas
fetal alcohol syndrome
type of twin that shares 1 placenta, 1 chorion, but has its own amniotic sac
monozygotic (maternal) twins
type of twin who fetus each has its own placenta, own chorion, and own amniotic sac
dizygotic (paternal) twins
type of twin where both fetuses share a placenta, chorion, and amniotic sac
conjoined twin
cells that secrete hCG
syncytiotrophoblasts
maternal component of the placenta
decidua basalis
where are the umbilical arteries/veins derived from
allantois
embryonic structure that gives rise to the ascending aorta and pulmonary trunk
truncus arteriosus
R common cardinal vein and R anterior cardinal vein come together to form what vessel in the newborn
SVC
characterized by a membranous septal defect causing initial L->R shunting which then later becomes R->L after the development of pulmonary HTN
Eisenmenger's syndrome
site of erythropoiesis in the embryo during weeks 3-8
yolk sac
site of erythropoiesis in the embryo during weeks 8-30
liver and spleen
site of erythropoiesis in the embryo during from weeks 28 and onward
bone marrow
blood entering the fetus passes through what vessel into the IVC in order to bypass hepatic circulation
ductus venosus
endogenous hormone whose decrease causes natural closure of the ductus arteriosus after birth
prostaglandins
thalami are derived from what primitive part of the brain
diencephalon
cerebral hemispheres are derived from what primitive part of the brain
telencephalon
the medulla is derived from what primitive part of the brain
myelencephalon
the pons and cerebellum are derived from what primitive part of the brain
metencephalon
neural tube defects are suggested by an increase in what hormone
AFP
usually the only physical sign suggesting spina bifida occulta
a patch of hair over the lesion
characterized by cape-like bilateral loss of pain and temperature sensation in the upper extremities with preservation of touch
syringomyelia
genetic disorder caused by failure of the 1st arch of the neural crest to migrate; characterized by mandibular hypoplasia and facial abnormalities
treacher collins
CN responsible for sensation on the ant. 2/3 of the tongue
CN V3
CN responsible for taste on the ant. 2/3 of the tongue
CN VII
CN responsible for taste on the post. 1/3 of the tongue
CN IX
CN responsible for sensation of the post. 1/3 of the tongue
CN IX
normal adult remnant of the thyroglossal duct
foramen cecum
caused by failed fusion between the maxillary and medial nasal processes
cleft lip
caused by failed fusion between the lateral palantine process, nasal septum, and median palatine process
cleft palate
during the 10th week of embryogenesis, the midgut rotates around what vessel
SMA
characterized by extrusion of abdominal contents through abdominal folds not covered by peritoneum
gastroschisis
characterized by the herniation of abdominal contents into the umbilical cord which is covered by peritoneum
omphalocele
characterized by cyanosis, choking and vomiting upon feeding, air bubble in the stomach on xray, polyhydramnios, pneumonitis, and the inability to pass a nasogastric tube into the stomach
tracheoesophageal fistula
congenital GI defect noted for usually only occuring in first-born males
congenital pyloric stenosis
caused by the failure of fusion of the ventral and dorsal parts of the pancreas by week 8
pancreas divisum
functions of the fetal kidney for the 1st trimester and then goes on to contribute to the male genital system
mesonephros
gives rise to the ureter, renal pelvis, calyces, and collecting ducts
ureteric bud
MOST common site of obstruction in the fetus (leads to hydronephrosis)
ureteropelvic junction (UPJ)
characterized by bilateral renal agenesis, oligohydramnios, limb deformities, facial deformities, and pulmonary hypoplasia
Potter's syndrome
cause of Potter's syndrome
malformation of the ureteric bud
characterized by fusion of the inferior poles of the kidney
horseshoe kidney
horseshoe kidney commonly become trapped under what vessel
IMA
paramesonephric ducts give rise to what gender development
female
the duct in which all male internal genital structures (other than the prostate) develop from
mesonephric (wolffian) duct
characterized by urinary tract abnormalities and infertility; caused by incomplete fusion of the paramesonephric ducts
bicornuate uterus
labia majora are homologous to what male structure
scrotum
the prostate gland is homologous to what female structure
paraurethral (skene's) glands
bulbourethral glands in the male are homologous to what female structure
Bartholin (greater vestibular) glands
difference between hypospadias and epispadias
in hypospadias, the urethra opens on the ventral side of the penis; in epispadias, the urethra opens on the dorsal side of the penis
female remnants of the gubernaculum
ovarian ligament and round ligament (of the uterus)
processus vaginalis is obliterated in what gender
females (becomes the tunica vaginalis in males)