Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A genetically and clinically heterogeneous group of slowly progressive neurological disorders which in the pure form is characterized by pyramidal signs (weakness, spasticity, brisk tendon reflexes, and extensor plantar responses) predominantly affecting the lower limbs and with possible association of sphincter disturbances and deep sensory loss; and in the complex form by the addition of variable neurological or non-neurological features. Disease data Klasyfikacja Clinical group Synonimy Familial spastic paraplegia Choroba Strümpella i Lorraina HSP Rodzinna paraplegia spastyczna SPG HSP Hereditary spastic paraparesis SPG Strümpell-Lorrain disease Kod ORPHA 685 Kod OMIM - Kod ICD10 G11.4 Kod ICD11 8B44.0 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl