Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A partial autosomal trisomy characterized by developmental delay and intellectual disability, generalized hypotonia, postnatal growth retardation, variable brain and heart anomalies and dysmorphic features, including frontal bossing, round face, full cheeks, low-set ears, broad nasal bridge, short nose with anteverted nares, long philtrum, thin upper lip vermilion, and everted, thick lower lip. Unspecific associated congenital anomalies have also been reported. Disease data Klasyfikacja Malformation syndrome Synonimy Duplication 12p Duplikacja 12p Kod ORPHA 1699 Kod OMIM - Kod ICD10 Q92.3 Kod ICD11 LD41.B1 *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