ok i have some questions, any help would be great:
1. can some one this question, i don't understand this statement: "differing phenotypes based on paternal are most compatible with which of the following genetic mechanisms: a. anticipation b. tri nucelo repeat expansion c. imprinting d. loss of heterozygosity e. pleiotropy
C. imprinting (I think)
3. Lower threshold for liability in males than females, woman has dz, which relative is at greatest risk for dz? (I'm really bad with genetics, ugh).
look at the rest of the thread, people are saying it's a female baby, higher risk in her brother (1st born males have highest occurrence)
5. Swollen third nipple...which cell type is present? I thought neutrophils for acute inflammation...is it epi cells?
epithelial
7. Salk/Sabin: common link is production of what? CTL in circ?
Ab in circ...the difference that is important here is that the PO vaccine induces production of IgA, but both have circulating Ab
8. cholinesterase-i aids memory by targeting synapses where?
I don't remember the specific answer but it was the only one going to the cerebral cortex
10. Alcoholic with sever hyponat, tx, then develops slurred speech + mod. weakness in all extremities w/ sensation in tact. Where is the lesion?
Brainstem-I believe they were hinting at central pontine myelinolysis
11. AA male with hypochrom/microcytic anemia, norm Fe, brother dx with anemia at 20yo, what do you do? I put BM biopsy...so it's an electrophoresis. How would the RDW not be high for all the variation in size with the sickled RBCs?
That's because it's not sickle cell, it's thalassemia (if I am remembering this correctly)
12. Baby with diaper rash...what is going on here?
Kawasaki disease...so the one with vasculitis & coronary artery aneurysm
Thanks for any help, much appreciated!