Neurol. praxi. 2010;11(6):410-414
Multiple sclerosis (MS) is a heterogenous disease of central nervous system (CNS) with variable clinical signs. The onset of MS may
imitate the whole scale of different, not only neurological diseases and detailed differential diagnosis of it is recommended. The goal
of our study was to alert the possible coincidence of MS and inherited thrombophilia, the difficulties in diagnosis of clinically isolated
syndrome suspected from MS in patients with inherited thrombophília and analyse its possible complications in patients with clinically
definitive MS. Out of 412 MS patients from both MS centres in Košice and in Prešov we have found in retrospective analyses 24 ones with
this deficiency of haemosthasis. Due to our information, this topic was not researched in Slovak MS population so far.
Published: December 31, 2010 Show citation