Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare neurologic disorder characterized by a unique non-REM and REM parasomnia with sleep breathing dysfunction, gait instability and repetitive episodes of respiratory insufficiency, as well as autoantibodies against IgLON5. Patients may present stridor, chorea, limb ataxia, abnormal ocular movements, and bulbar symptoms (i.e. dysphagia, dysarthria, episodic central hypoventilation) with normal brain MRI. Excessive day sleepiness and cognitive deterioration have also been reported. Disease data Klasyfikacja Disease Synonimy Anti-IgLON5 disease Anti-IgLON5 syndrome Anti-IgLON5 disease Anti-IgLON5 syndrome Kod ORPHA 420789 Kod OMIM - Kod ICD10 G04.8 Kod ICD11 - *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