- Hereditary Neuropathy with Pressure Palsies
- Neurology: HNPP
Универсальный русско-английский словарь. Академик.ру. 2011.
Универсальный русско-английский словарь. Академик.ру. 2011.
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