Hereditary Neuropathy with Pressure Palsies

Hereditary Neuropathy with Pressure Palsies
Neurology: HNPP

Универсальный русско-английский словарь. . 2011.

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  • hereditary neuropathy with liability to pressure palsies — (HNPP) an autosomal dominant neuropathy due to deletion of the PMP22 gene (locus: 17p11.2), which encodes a specific myelin protein; it is allelic with Charcot Marie Tooth disease type IA , which is caused by duplication of that gene. It is… …   Medical dictionary

  • Peripheral neuropathy — Neuropathy redirects here. For other uses, see Neuropathy (disambiguation). Not to be confused with Nephropathy. Peripheral neuropathy Classification and external resources …   Wikipedia

  • Neuropathy — Any and all disease or malfunction of the nerves. * * * 1. A classical term for any disorder affecting any segment of the nervous system. 2. In contemporary usage, a disease involving the cranial nerves or the peripheral or autonomic nervous …   Medical dictionary

  • tomaculous neuropathy — hereditary n. with liability to pressure palsies …   Medical dictionary

  • HNPP — hereditary neuropathy with liability to pressure palsies …   Medical dictionary

  • HNPP — • hereditary neuropathy with liability to pressure palsies …   Dictionary of medical acronyms & abbreviations

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  • Peripheral myelin protein 22 — Peripheral myelin protein 22, also known as PMP22, is a human gene.The integral membrane protein encoded by this gene is a hydrophobic, tetraspan glycoprotein expressed mainly in Schwann cells and is a major component of compact myelin in the… …   Wikipedia

  • COX10 — homolog, cytochrome c oxidase assembly protein, heme A: farnesyltransferase (yeast), also known as COX10, is a human gene.cite web | title = Entrez Gene: COX10 COX10 homolog, cytochrome c oxidase assembly protein, heme A: farnesyltransferase… …   Wikipedia


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