Background: This study aims to collect local Malaysian data regarding the ophthalmic
features and complications in craniosynostosis patients who attended the Combined …

Among the craniosynostosis syndromes, Pfeiffer syndrome is notable because of high
mortality and the need for multiple surgical interventions. However, it is variable in severity …

El síndrome de Pfeiffer es un trastorno autosómico dominante infrecuente que afecta
aproximadamente 1 de cada 100,000 recién nacidos vivos, y en general se acompaña de …

The monobloc advancement with distraction is a treatment modality for syndromic
craniosynostosis, to correct exorbitism, upper airway compromise and malocclusion. In this …

Objectives: Identify the etiology of Pfeiffer syndrome. Describe the evaluation of Pfeiffer
syndrome. Outline the treatment and management options available for Pfeiffer syndrome …

Background Pfeiffer syndrome is a rare, genetic condition characterized by craniosynostosis
and midface hypoplasia, with resultant ophthalmic sequelae. The gold standard of treatment …

The male propositus was the first child of a healthy unrelated couple. The mother was 31
years old. There was no family history of congenital malformations. The pregnancy was …

Background: Craniofacial structures have an intimate relationship with the central nervous
system in the embryologic development period and the developmental abnormalities of the …

Discussion The exact incidence of Pfeiffer syndrome is unknown. It is estimated to be
1/100,000 births [3]. In 1993, Cohen [4] classified Pfeiffer syndrome into three sub-types …

Craniosynostosis occurring in conjunction with other genetic anomalies is classified as
syndromic craniosynostosis. Syndromes commonly associated with craniosynostosis …