CARPENTER SYNDROME : HEREDITARY OCULAR DISEASE

Abstract The genetic types of craniosynostosis will be divided into four groups: isolated craniosynostosis, craniosynostosis with birth defect, craniosynostosis with congenital defect and birth defect, and craniosynostosis with alternative corporeal abnormalities. Acrocephalopolysyndactyly or Carpenter syndrome consists of craniosynostosis, short fingers, soft tissue birth defect, syndactyly,, inborn cardiopathy, hypogenitalism, obesity, and herniation. As several as common fraction of the patients have a point of intellectual impairment. The etiology of backwardness during this syndrome has not been explored. A patient is reportable with the options of Carpenter syndrome WHO has profound organic process delay and cerebral malformations incontestable by resonance imaging and computed axial tomography. as a result of backwardness isn't associate invariant feature of this syndrome or alternative craniosynostosis syndromes, neuroradiologic examination might facilitate in predicting the intellectual outcome in these patients. Key Words – craniosynostosis, syndactyly, syndactyly, hypogenitalism.