Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare primary bone dysplasia characterized by severe mesomelic shortness particularly of the lower limbs with distinctive triangular or rhomboid-shaped tibiae and fibulae, accompanied by bony protuberances and skin dimples. Additional manifestations include radioulnar synostosis, dislocation of the radial head, abnormalities of the hands (such as oligosyndactyly or fusiform-shaped fingers) and feet (pes equinovarus, synostoses of tarsals/metatarsals and phalanges), and dysmorphic facial features. Disease data Klasyfikacja Malformation syndrome Synonimy Mesomelic dwarfism, Nievergelt type Zespół Nievergelta Nievergelt syndrome Kod ORPHA 2633 Kod OMIM 163400 Kod ICD10 Q78.8 Kod ICD11 LD24.A *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