Management of Seckel Syndrome with Cerebral Aneurysms: Favorable Outcomes

A 13-year-old boy affected by Seckel syndrome (SS) with multiple intracranial aneurysms is reported. SS is a rare, autosomal recessive syndrome characterized by severe intrauterine and postnatal growth retardation, microcephaly, and typical facial appearance with a beaklike protrusion of the midface (bird-headed). His diagnostic workup was done based on a significant family history and his phenotypic appearance of SS. The aneurysms were surgically treated, and the favorable outcomes were discussed.