Acalvaria defined as absent skull bones, is an extremely rare congenital anomaly with only a handful of cases reported in literature. In this report we presented a male newborn case of acalvaria referred to our hospital (Shahid Motahari hospital of Urmia, Iran). The condition per se has been described as having high mortality rate. Very few living cases, less than ten, have been reported till now.

Chiari I malformation may not be congenital, but may be acquired as a consequence of skull deformities and other associated intracranial factors in patients with craniosynostosis. Pfeiffer syndrome is one of the many conditions associated with Chiari I malformation. Premature fusion of multiple cranial sutures and cloverleaf skull (kleeblattschädel deformity) are often observed in the calvaria ...

This article reviews the development of research in field craniosynostosis from a bibliometric standpoint. Craniosynostosis is malformation occurring during early skull, when one or more sutures close too early, causing problems with normal brain and skull growth. Research this has developed clinical case descriptions, to genetic discoveries responsible for malformations onwards developing soph...

Apert syndrome (AS) is a common genetic syndrome in humans characterized with craniosynostosis. Apert patients and mouse models showed abnormalities in sutures, cranial base and brain, that may all be involved in the pathogenesis of skull malformation of Apert syndrome. To distinguish the differential roles of these components of head in the pathogenesis of the abnormal skull morphology of AS, ...

BACKGROUND Infantile cortical hyperostosis is characterised by hyperirritability, acute inflammation of soft tissue, and profound alterations of the shape and structure of the underlying bones, particularly the long bones, mandible, clavicles, or ribs. CASE PRESENTATION We report on a clinical case of a 3-months-old baby girl of non-consanguineous parents. Multiple long bone swellings were th...

According to some studies, the number of addicted females in reproductive ages has been increased. The present study was designed to investigate the effect of oral morphine consumption on the development of CNS and body growth in rats. For this purpose, female Sprauge-Dawley rats were divided into control and experimental groups (20 animals in each group). Maintenance dose of morphine (0/4 mg/m...

According to some studies, the number of addicted females in reproductive ages has been increased. The present study was designed to investigate the effect of oral morphine consumption on the development of CNS and body growth in rats. For this purpose, female Sprauge-Dawley rats were divided into control and experimental groups (20 animals in each group). Maintenance dose of morphine (0/4 mg/m...

OBJECTIVE To examine the association between severity of scaphocephalic skull malformation and neurodevelopmental status prior to cranioplasty. DESIGN AND PARTICIPANTS Seventy-five infants with single-suture sagittal craniosynostosis (median age, 4.5 months) referred to the Infant Learning Project, a prospective, multisite, longitudinal study to evaluate neurocognitive development. MAIN OUT...