Alright, time for Point 2 on my Blurbs: My issue with the genetics course and my recommendations to the faculty.
So this course was to introduce us to medical genetics. I was on the M1 liaison committee for this course and it was honestly somewhat frustrating hearing the excuses made by the faculty (valid excuses though they were). Most of their arguments boiled down to "We didn't have enough time. We had to cut something and we decided to cut that." -_- In its current iteration, this course doesn't really help us as future clinicians recognize and diagnose genetic illnesses, nor really help us track them through family history. Some diseases and important points were highlighted, but certainly not enough to be useful. Apparently there's a lot of "turf war" going on between classes and allotting time. Ugh, inter-department politics (not to mention inner-department politics). Fact is, there are things they could've done to improve the quality of this course given it's very short class-time.
My recommendations on the eval were as follows:
- Simplify and combine the lectures on transcription and translation into a single lecture.
- Simplify the cyclin/CDK material and combine the lectures on mitosis and meiosis into a single lecture.
- Have a lecture on Mendelian genetics and non-Mendelian genetics.
- Have a lecture on epigenetics.
- Have a lecture on creating pedigrees and emphasize their importance in medicine (or make this a short online tutorial).
- Have a lecture on genetic counseling: who are genetic counselors, what they do, when to refer, etc (or make this a short online tutorial).
- Have a lecture on the ethics of genetics and genetics research (or make this a short online tutorial).
- Have 1-2 lectures on cancer genetics. The first can focus on the genetics of cancer (e.g. Knudson's two-hit hypothesis, transformation from normal cells to hyperplasia to malignancy, a little bit of pathology), and the second lecture can focus on specific genetic cancers (e.g. BRCA1/2 and breast cancer, APC and familial adenomatous polyposis, p53 and Li-Fraumeni).
- Reorganize the lecture on Huntington's corea, Duchenne's muscular dystrophy, and cystic fibrosis to highly other genetic diseases (specifically Huntington's corea, Prader-Willi, Angelman's, and sickle-cell anemia). DMD and cystic fibrosis have been repeatedly covered again and again in other lectures.
- Simplify the development section of this course. Combine weeks 1 and 2 into a single lecture, and weeks 3 and 4 into a single lecture.
- Enforce greater communication between faculty lecturers so that the same topic isn't lectured on over and over again (i.e. telomerase, DMD, and cystic fibrosis).
If they even did 1/3 of the recommendations above I believe this course would've been greatly improved next year. But it's not like it matters much in the long run, as in 2-3 years there's going to be a massive shift in the curriculum into something entirely new and unrecognizable, and the current classes we now take will be abolished for a new system. That could be interesting . . .
So this course was to introduce us to medical genetics. I was on the M1 liaison committee for this course and it was honestly somewhat frustrating hearing the excuses made by the faculty (valid excuses though they were). Most of their arguments boiled down to "We didn't have enough time. We had to cut something and we decided to cut that." -_- In its current iteration, this course doesn't really help us as future clinicians recognize and diagnose genetic illnesses, nor really help us track them through family history. Some diseases and important points were highlighted, but certainly not enough to be useful. Apparently there's a lot of "turf war" going on between classes and allotting time. Ugh, inter-department politics (not to mention inner-department politics). Fact is, there are things they could've done to improve the quality of this course given it's very short class-time.
My recommendations on the eval were as follows:
- Simplify and combine the lectures on transcription and translation into a single lecture.
- Simplify the cyclin/CDK material and combine the lectures on mitosis and meiosis into a single lecture.
- Have a lecture on Mendelian genetics and non-Mendelian genetics.
- Have a lecture on epigenetics.
- Have a lecture on creating pedigrees and emphasize their importance in medicine (or make this a short online tutorial).
- Have a lecture on genetic counseling: who are genetic counselors, what they do, when to refer, etc (or make this a short online tutorial).
- Have a lecture on the ethics of genetics and genetics research (or make this a short online tutorial).
- Have 1-2 lectures on cancer genetics. The first can focus on the genetics of cancer (e.g. Knudson's two-hit hypothesis, transformation from normal cells to hyperplasia to malignancy, a little bit of pathology), and the second lecture can focus on specific genetic cancers (e.g. BRCA1/2 and breast cancer, APC and familial adenomatous polyposis, p53 and Li-Fraumeni).
- Reorganize the lecture on Huntington's corea, Duchenne's muscular dystrophy, and cystic fibrosis to highly other genetic diseases (specifically Huntington's corea, Prader-Willi, Angelman's, and sickle-cell anemia). DMD and cystic fibrosis have been repeatedly covered again and again in other lectures.
- Simplify the development section of this course. Combine weeks 1 and 2 into a single lecture, and weeks 3 and 4 into a single lecture.
- Enforce greater communication between faculty lecturers so that the same topic isn't lectured on over and over again (i.e. telomerase, DMD, and cystic fibrosis).
If they even did 1/3 of the recommendations above I believe this course would've been greatly improved next year. But it's not like it matters much in the long run, as in 2-3 years there's going to be a massive shift in the curriculum into something entirely new and unrecognizable, and the current classes we now take will be abolished for a new system. That could be interesting . . .

