Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare, genetic, congenital limb malformation syndrome characterized by unilateral or bilateral fibular aplasia/hypoplasia, tibial campomelia, and lower limb oligosyndactyly involving the lateral rays. Upper limb oligosyndactyly and cleft lip/palate may also be associated. Disease data Classification Malformation syndrome Synonyms Fibular aplasia-tibial campomelia-oligosyndactyly syndrome Zespół Hecht i Scotta Hecht-Scott syndrome ORPHA code 2492 OMIM code - ICD10 code Q87.2 ICD11 code - *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