BASAL CELL NEVUS (GORLIN) SYNDROME WITH A NOVEL HETEROZYGOUS DELETION FRAMESHIFT MUTATION (C.959DELC, P.VAL322 PHE FSX2) IN THE PTCH1 GENE ASSOCIATED WITH EPIRETINAL MEMBRANE, ODONTOGENIC KERATOCYSTS AND WITHOUT SKIN LESIONS AND FALX CEREBRI CALCIFICATION için istatistikler