Fine–Lubinsky syndrome is a rare genetic disorder which is characterized by ocular and hearing problems, speech and developmental delay, short stature, intellectual disabilities and facial dysmorphisms. __TOC__
Presentation
Symptoms may vary from person to person, but they generally are (but are not limited to): Intellectual disabilities of varying degree Congenital hearing loss Congenital cataracts and/or glaucoma Brachycephaly Brain abnormalities (often leading to behavioral problems) Finger abnormalities Cleft palate Flat face Ptosis Long philtrum Small mouth Short nose Microstomia Scrotum hypoplasia
Etiology
Although most cases of Fine–Lubinsky syndrome are sporadic, a case report of two siblings with this syndrome was published, suggesting that it is caused by autosomal recessive mutations in the MAF gene. Diagnosis
Treatment
References