We reviewed 25 patients ascertained through the finding of trigonocephaly/metopic synostosis as a prominent manifestation. In 16 patients, trigonocephaly/metopic synostosis was the only significant finding (64%); 2 patients had metopic/sagittal synostosis (8%) and in 7 patients the trigonocephaly was part of a syndrome (28%). Among the nonsyndromic cases, 12 were males and 6 were females and th...

Beutler, E., and Baluda, M. C. (1966). Improved method for measuring galactose-l-phosphate uridyl transferase activity of erythrocytes. Clinica Chimica Acta, 13, 369-379. Federhol, M. K. (1969). Quantitative studies on the inherited variants of serum alpha-l-antitrypsin. Scandinavian Journal of Clinical and Laboratory Investigation, 23, 97-103. Lejeune, J., Berger, R., Lafourcase, J., and Retho...

OBJECT Chiari malformation (CM) Type I is frequently associated with craniosynostosis. Optimal management of CM in patients with craniosynostosis is not well-established. The goal of this study was to report on a series of pediatric patients with both craniosynostosis and CM and discuss their management. METHODS The authors searched the medical records of 383 consecutive patients treated for ...

OBJECTIVE Sagittal synostosis is the most common form of isolated craniosynostosis. Although some centers have reported extensive experience with this condition, reports focused on a single center. In 2017, Synostosis Research Group (SynRG), multicenter collaborative network, was formed to study Here, authors report their early treating sagittal in network. The goals were describe practice patt...

BACKGROUND Presentation of proximal radioulnar synostosis varies from cosmetic concerns with no functional limitations to significant pronation deformity which hampers activities of daily living. Surgical management must be considered based on the position of the forearm and functional limitations. We describe the surgical technique, results, and complications of excision of the radial head alo...

Congenital proximal radioulnar synostosis is a rare congenital anomaly that can be extremely disabling, especially when it occurs bilaterally or if there is severe hyperpronation. Currently, osteotomy to achieve a neutral or slightly pronated position is widely accepted for the management of patients who have severe pronation. The present study evaluates the result of two-stage double-level rot...

Beutler, E., and Baluda, M. C. (1966). Improved method for measuring galactose-l-phosphate uridyl transferase activity of erythrocytes. Clinica Chimica Acta, 13, 369-379. Federhol, M. K. (1969). Quantitative studies on the inherited variants of serum alpha-l-antitrypsin. Scandinavian Journal of Clinical and Laboratory Investigation, 23, 97-103. Lejeune, J., Berger, R., Lafourcase, J., and Retho...

Deformities of the cranium in patients with nonsyndromic single-suture synostosis occur because of growth restriction at fused sutures and growth over compensation at normal sutures. Traditional surgery includes ostectomies of the synostotic suture to release these restricted areas and osteotomies to enable immediate cranial remodeling. In the process of reshaping the cranium, traditional appro...