Hunter-McAlpine craniosynostosis

Hunter-McAlpine craniosynostosis is characterized by craniosynostosis, intellectual deficit, short stature, facial dysmorphism (oval face with almond-shaped palpebral fissures, droopy eyelids and a small nose) and minor distal anomalies. It has been described in 10 patients. Transmission is autosomal dominant and the syndrome is associated with partial duplication of the long arm of chromosome 5 (5q35-5qter).

Also known as: Hunter-McAlpine craniosynostosis syndrome, Hunter-McAlpine syndrome, craniosynostosis, mental deficiency, almond-shaped palpebral fissures, downturned mouth, mild acral-skeletal anomalies, and short stature

1 clinical trial for this condition and its sub-types, 0 tagged with Hunter-McAlpine craniosynostosis itself.