Video from Ninja Nerd on YouTube

1.1.4 Relate organelle dysfunction to disease, for example lysosomal storage disorders and mitochondrial disorders.

Why this video

It explains lysosome biology and the pathophysiology of key lysosomal storage diseases resulting from acid hydrolase deficiencies, including Tay-Sachs, Gaucher, and Niemann-Pick diseases.

Part of this line

Covers part of this objective. It leaves out: It focuses solely on lysosomal storage diseases, omitting mitochondrial disorders and diseases of other organelles.

Heads up

This course only expects the general mechanism of lysosomal storage disorders along with Tay-Sachs and Gaucher diseases in this introductory unit, deferring detailed sphingolipid degradation pathways to lipid metabolism.

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