گزارش یک مورد سندرم آپرت

Âpert syndrome is a case syndrome with an incidence of about 16 in 1,000,000 live births. Ït is classified with the Âcrocephalosyndactyly syndromes, which is cranyosynostosis in combination with syndactyly in hands and feet. The other common clinical manifestations in Âpert Syndrome are acrocephaly, Turibrachycephaly, syndactyly on hands and feet, wide Tumb, ante mongoloid polpebral fissure, cleft palate, proptosis and under development of mid face. This is a case report of a neonate with clinical manifestations of Âpert syndrome.