Apert syndrome: a rare congenital anomaly and experience from a low-resource country: a case report and review of the literature.

Background: Apert syndrome is a congenital condition characterized by coronal craniosynostosis, ex-orbitism, midface hypoplasia as well as symmetric syndactyly of both feet and hands. Apert syndrome is linked by autosomal dominant inheritance to fibroblast growth factors receptor gene alteration. Case presentation: We present the case of a 20-month-old African boy who exhibited the characteristic facial features of Apert syndrome. Additionally, the child presented with syndactyly of both the fingers and toes. He was born to non-consanguineous parents, with the father being 33 years old at the time of the child's birth. A skull X-ray revealed an increased anteroposterior diameter of the skull, consistent with the cranial abnormalities associated with Apert syndrome. Further imaging of the hands and feet confirmed the pathognomonic syndactyly characteristic of the condition. The patient successfully underwent a series of surgeries to release the syndactyly in both his right and left hands. These surgical interventions have significantly improved the functionality of his hands. Conclusions: There is a paucity of information about Apert syndrome in Africa. Therefore, in order to enhance strong advocacy of this condition in Africa, more cases should be reported. [ABSTRACT FROM AUTHOR]