Fah Bouaré, Mohammad Hassan A Noureldine, Farouk Hajhouji, Houssine Ghannane, George I Jallo, Said Ait Benali
Carpenter's syndrome or acrocephalopolysyndactyly type II is a rare genetic autosomal recessive disease, with an incidence estimated at 1 per 1 million births. Common findings of a brachydactyly, polysyndactyly, and a trefoil-like skull with extreme brachycephaly due to fusion of the bilateral coronal, sagittal and lambdoid sutures. We report a 12-month-old male who was referred to our care for evaluation of a craniofacial deformity-a trefoil-like skull, flattened and receding forehead, bulging of temporal bones, hypertelorism, exorbitism, and polysyndactyly in the upper and lower limbs and psychomotor delay...
April 2022: Child's Nervous System: ChNS: Official Journal of the International Society for Pediatric Neurosurgery