Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare multiple congenital anomalies/dysmorphic syndrome characterized by a variable combination of dental, cutaneous, ocular, and bone abnormalities, including pyramidal and fused molar roots, taurodontism, an abnormal upper lip without a cupid's bow and thickened and wide philtrum, juvenile glaucoma, syndactyly, and clinodactyly. There have been no further descriptions in the literature since 1973. Disease data Klasyfikacja Malformation syndrome Synonimy Ackerman fused molar roots syndrome Pyramidal molar - jaskra - nieprawidłowa warga górna Kod ORPHA 2561 Kod OMIM 200970 Kod ICD10 K00.2 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