Alport Syndrome | USMLE Step 1 Mnemonic
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- เผยแพร่เมื่อ 5 ส.ค. 2024
- Alport syndrome is an X-linked dominant disorder that is characterized by a mutation in type IV collagen. As a result of this defect, patients with Alport syndrome have defective basement membranes in various organs. Defects in the glomerular basement membrane lead to glomerulonephritis, which manifests as a "basket-weave" pattern on electron microscopy. Alport syndrome patients also develop a number of eye problems, as basement membranes are found in the lens capsule and retina. Such eye problems include cataracts, retinopathy, and lens dislocation. Finally, defects in the cochlear basement membrane lead to sensorineural deafness in patients with Alport syndrome.
Learn about Alport syndrome and other medical school topics with Pixorize's USMLE Step 1 mnemonics. Part of our Collagen playlist for the USMLE Step 1 exam.
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Isn' t it comes under X link recessive? 🤔
No.. it is X linked dominant..
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Its x linked reccesive bro not the x linked dominant inheritence
Actually, it can be caused by both X-linked (85% cases) or autosomal mode of inheritance and in that, X-linked dominant is more common than X-linked recessive.
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