familial spastic paraplegia

familial spastic paraplegia
hereditary spastic p.

Medical dictionary. 2011.

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  • familial spastic paraparesis — hereditary spastic paraparesis see under paraplegia …   Medical dictionary

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  • SPG3A — Spastic paraplegia 3A (autosomal dominant), also known as SPG3A, is a human gene.cite web | title = Entrez Gene: SPG3A spastic paraplegia 3A (autosomal dominant)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… …   Wikipedia

  • FSP — familial spastic paraplegia; femoral hole sagittal positioning; fibrinogen split products; fibrin split products; fine suspended particles …   Medical dictionary

  • FSP — • familial spastic paraplegia; • femoral hole sagittal positioning; • fibrinogen split products; • fibrin split products; • fine suspended particles …   Dictionary of medical acronyms & abbreviations

  • NIPA1 — Non imprinted in Prader Willi/Angelman syndrome 1 Identifiers Symbols NIPA1; FSP3; MGC102724; MGC35570; SPG6 External IDs …   Wikipedia

  • Poikilodermie — (dt. ‚bunte Haut‘) ist die unspezifische Sammelbezeichnung einer Gruppe von Hautkrankheiten. Poikilodermien sind epidermale diffuse Atrophien, die zusammen mit erweiterten Kapillargefäßen der Haut (Teleangiektasie) und einer Hyper oder einer… …   Deutsch Wikipedia

  • AD-FSP — autosomal dominant familial spastic paraplegia …   Medical dictionary

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