Summary Background Neurofibromatosis type 1 (NF1) is a multisystem genetic disorder,
predisposing development of benign and malignant tumours. Given the oncogenic potential …

Background: Previous research has highlighted the gender-based disparities present
throughout the field of surgery. This study aims to evaluate the breadth of the issues facing …

Background: No reviews or guidelines are available on evidence-based treatment for the
multidisciplinary approach in Treacher Collins syndrome. The authors' aim is to provide an …

Carpenter syndrome is a pleiotropic disorder with autosomal recessive inheritance, the
cardinal features of which include craniosynostosis, polysyndactyly, obesity, and cardiac …

This guideline for care of children with craniosynostosis was developed by a national
working group with representatives of 11 matrix societies of specialties and the national …

Craniosynostosis and supernumerary teeth most often occur as isolated developmental
anomalies, but they are also separately manifested in several malformation syndromes …

Craniosynostosis, the premature fusion of the cranial sutures, is a heterogeneous disorder
with a prevalence of∼ 1 in 2,200 (refs.,). A specific genetic etiology can be identified in∼ …

Introduction Craniosynostosis represents premature closure of cranial sutures. Prevalence is
approximately 3.1–6.4 in 10.000 live births, which is reportedly rising. This epidemiologic …

Background: The application of a new approach is presented, percutaneous aponeurotomy
and lipofilling, which is a minimally invasive, incisionless alternative to traditional flap …

Metopic synostosis is thought to have an incidence of about 1 in 15,000 births. Traditionally,
this makes it the third most frequent single-suture craniosynostosis, after scaphocephaly (1 …