Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by congenital cataract, sensorineural hearing loss, developmental delay with variable degrees of intellectual disability, seizures, short stature, brachycephaly, and dysmorphic facial features (such as flat facial appearance, ptosis, short nasal tip, long philtrum, low-set and posteriorly rotated ears, and small mouth). Additional reported manifestations are skeletal abnormalities, nail dystrophy, mammary gland hypoplasia, and autism spectrum disorder. Disease data Klasyfikacja Malformation syndrome Synonimy Brachycephaly-deafness-cataract-intellectual disability syndrome Krótkogłowie - głuchota - zaćma - niepełnosprawność intelektualna Brachycephaly-hearing loss-cataract-intellectual disability syndrome Fine-Lubinsky syndrome Kod ORPHA 1272 Kod OMIM 601353 Kod ICD10 Q87.8 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