A - nucleus ( with nucleolus inside ) B - mitochondria C - RER ( you can see attached ribosomes ) D - ?? may be lysosomes E - glycogen granules
This patient presents with a mitochondrial myopathy since the disorder is inherited from the mother. Mitochondrial myopathies show โragged red fibersโ on muscle biopsy due to the accumulation of diseased mitochondria in the subsarcolemma of the muscle fiber.
Does anyone know what are A, C, D? For C not sure if it's pointing to the ribosomes on RER.
(I'm assuming E is glycogen granules based on a comment below!)
does anyone know what the structure E is pointing to?
Anyone find a problem with the stem? Seems to me that it doesn't help to state "however, his father's sister and children are unaffected". We already know the mutation runs in the mother's side, right? It seems like that statement doesn't discard nor confirm any inheritance pattern. Why would we care about the patient's father's side?
submitted by โusmle11a(102)
https://www.youtube.com/watch?v=k0YqEpA-62A
guys this video explains alot