Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition 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 Classification Malformation syndrome Synonyms Brachycephaly-deafness-cataract-intellectual disability syndrome Krótkogłowie - głuchota - zaćma - niepełnosprawność intelektualna Brachycephaly-hearing loss-cataract-intellectual disability syndrome Fine-Lubinsky syndrome ORPHA code 1272 OMIM code 601353 ICD10 code Q87.8 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