Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition 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 Classification Malformation syndrome Synonyms Mesomelic dwarfism, Nievergelt type Zespół Nievergelta Nievergelt syndrome ORPHA code 2633 OMIM code 163400 ICD10 code Q78.8 ICD11 code 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