Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare central nervous system malformation characterized by a fluid-filled longitudinally oriented cavity (syrinx) within the spinal cord, which may or may not communicate with the central canal, does not have an ependymal lining, and is either idiopathic or seen as a familial malformation. Clinical manifestations in symptomatic patients include neuropathic pain, as well as sensory and motor disturbances. Typical presentations may be cape-like loss of pain and temperature sensation along the torso and arms, or disproportionately greater motor impairment in upper compared to lower extremities. Disease data Klasyfikacja Morphological anomaly Synonimy Congenital syringomyelia Wrodzona jamistość rdzenia Kod ORPHA 99856 Kod OMIM - Kod ICD10 Q06.4 Kod ICD11 8D66.0 *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