Neurol. pro Praxi, 2006; 3: 147-152

Dědičné periferní neuropatie

MUDr. Jana Haberlová1, MUDr. Radim Mazanec PhD2, MUDr. Pavel Seeman Ph.D2
1 Klinika dětské neurologie 2. LF UK a Centrum pro epilepsie FN Motol, Praha
2 Neurologická klinika 2. LF UK a FN Motol, Praha

Dědičné periferní neuropatie jsou heterogenní skupinou geneticky podmíněných degenerativních chorob postihující periferní nervy. Patří mezi nejčastější dědičná nervosvalová onemocnění. Kauzální terapie dosud není známa, nicméně diagnostika a klasifikace se v posledních letech rychle vyvíjí a to hlavně díky novým objevům molekulární genetiky. Jde o skupinu chorob která nezkracuje délku života, výrazně však ovlivňuje jeho kvalitu. Je častou příčinou poruchy a někdy i ztráty chůze, často vede ke snížené pracovní schopnosti, později nezřídka i k plné invaliditě.

Keywords: klasifikace, fenotypy, diagnostika, terapie

Published: July 1, 2006  Show citation

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Haberlová J, Mazanec R, Seeman P. Dědičné periferní neuropatie. Neurol. praxi. 2006;7(3):147-152.
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References

  1. Dubourg O et al. Guidelines for diagnosis of hereditary neuroapthy with lability to preasure palsies. Neuromuscular Disord 2000; 10: 206-208. Go to original source... Go to PubMed...
  2. Garcia CA et al. Clinical variability in two pairs of identical twins with CMT 1A. Ann Neurol 1997; 41: 2090-2093.
  3. Harding AE et al. The clinical features of hereditary motor and sensory neuropathy types I and II. Brain 1980; 103: 259-280. Go to original source... Go to PubMed...
  4. Irobi J et al. Hot-spot residue in small heat-shock protein 22 causes distal motor neuropaty. Nat Genet 2004; 36/6: 547-8. Go to original source... Go to PubMed...
  5. Krajewski KM et al. Neurological dysfunction and axonal degeneration in Charcot -MarieTooth disease type 1A. Brain 2000; 123: 1516-1527. Go to original source... Go to PubMed...
  6. Kuhlenbaumer G et al. Mutation in SEPT 9 cause HNA. Nat Genet 2005; 37: 1044-6. Go to original source... Go to PubMed...
  7. Lawson VH et al. Clinical and electrophysiologic features of CMT2A with mutations in the mitofusin 2 gene. Neurology 2005; 65: 197-204. Go to original source... Go to PubMed...
  8. Meggouh F et al. The first de novo mutation of Cx32 gene associated with X-linked CMT. J Med Genet 1998; 35: 251-252. Go to original source... Go to PubMed...
  9. Mikesova E et al. Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosis. Neuromuscular Disord 2005; 15/11: 764-7. Go to original source... Go to PubMed...
  10. Passage E et al. Ascorbic acid treatment corrects the phenothype of a mouse model of CMT. Nature Medicine 2004; 10: 396-401. Go to original source... Go to PubMed...
  11. Sahenk Z et al. Neurotrophin-3 treatment promotes nerve regeneration and sensory improvement in CMT1A mouse models and in patiens. Neurology 2005; 65: 681-689. Go to original source... Go to PubMed...
  12. Seeman P et al. Hearing loss as the first feature of late onset axonal CMT disease due to a novel P0 mutation. Neurology 2004; 63: 733-735. Go to original source... Go to PubMed...
  13. Seeman P et al. Kongenitální hypomyelinizace v souvislosti s de-novo mutací genu pro PMP 22, 2001 - první prokázaný případ v ČR. Čes Slov Neurol Neurochir 2002; 65/98: 206-212.
  14. Seeman P et al. CMT gonosomálně dominantní typ CMT1X- první nálezy mutací v genu pro Cx32 v České republice. Čes Slov Neurol Neurochir 2000; 63/69: 219-225.
  15. Seeman P et al. Divergentní fenotypy choroby CMT: demyelinizační s infantilním začátkem a axonální s pozdním začátkem a zpomalenou fotoreakcí následkem různých mutací P0 genu. Čes Slov Neurol Neurochir 2004; 67/100: 321-329.
  16. Sereda MW et al. Therapeutic administration of anti-progesterone in a model of CMT 1A. Nature Medicine 2003; 9: 1533-7. Go to original source... Go to PubMed...
  17. Street VA et al., Mutation of putative protein degradation gene LITAF/SIMPLE in CMT disease 1C. Neurology 2003; 60: 22-26. Go to original source... Go to PubMed...
  18. Suter U et al. Disease mechanism in inherited neuropathies. Nature Reviews Neuroscience 2003; 4: 714-726. Go to original source... Go to PubMed...
  19. Shy M E et al. Reliability and validity of the CMT neuropathy score as a measure of disability. Neurology 2005; 64: 1209-1214. Go to original source... Go to PubMed...
  20. Verhoeven K et al. SPTLC1 mutation in twin sisters with HSN type I. Neurology 2004; 62: 1001-1002. Go to original source... Go to PubMed...




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