Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare dysostosis with predominant vertebral involvement characterized by paraspinal ligament ossification (most pronounced in the lower thoracic region), osteophytosis, marginal sacroiliac joint sclerosis, and punctate hyperkeratosis on the soles and palms. Patients may be asymptomatic or present mild to moderate back pain. There have been no further descriptions in the literature since 1969. Disease data Klasyfikacja Malformation syndrome Kod ORPHA 2206 Kod OMIM 106400 Kod ICD10 M48.1 Kod ICD11 LD24.H *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