Hereditary neuropathy with pressure palsies (HNPP): Difference between revisions
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'''Original Editor '''- User:Ravi Kumar | '''Original Editor '''- [[User:Ravi Kumar|Ravi Kumar]] | ||
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== Introduction == | == Introduction == | ||
Hereditary Neuropathy with Pressure Palsies (HNPP) is a rare genetic disorder that affects the peripheral nerves. It is inherited in an autosomal dominant manner meaning individuals have a 50% chance of passing it on to their children. | |||
The cause of HNPP is a mutation in the peripheral myelin protein 22 (PMP22) gene, which is responsible for producing a protein called PMP22. This protein plays a crucial role in the formation and maintenance of myelin, the protective covering around nerve fibers. Unfortunately in HNPP the mutation in the PMP22 gene leads to abnormalities in myelin structure and function resulting in nerve dysfunction. | |||
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Revision as of 14:31, 28 June 2023
Original Editor - Ravi Kumar
Top Contributors - Ravi Kumar
This article or area is currently under construction and may only be partially complete. Please come back soon to see the finished work! (Template:28/Template:06/{23}})
Introduction[edit | edit source]
Hereditary Neuropathy with Pressure Palsies (HNPP) is a rare genetic disorder that affects the peripheral nerves. It is inherited in an autosomal dominant manner meaning individuals have a 50% chance of passing it on to their children.
The cause of HNPP is a mutation in the peripheral myelin protein 22 (PMP22) gene, which is responsible for producing a protein called PMP22. This protein plays a crucial role in the formation and maintenance of myelin, the protective covering around nerve fibers. Unfortunately in HNPP the mutation in the PMP22 gene leads to abnormalities in myelin structure and function resulting in nerve dysfunction.
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