Apert syndrome is a rare condition, with a birth prevalence of approximately one in 65,000. This article provides an up-to-date review of the literature on Apert syndrome from a variety of …

Jun 7, 2016 · Apert syndrome is a rare condition, with a birth prevalence of approximately one in 65,000. This article provides an up-to-date review of the literature on Apert syndrome from a …

In the PubMed accessible literature, information on the characteristics of interdisciplinary orthodontic and surgical treatment of patients with Apert syndrome is rare. The aim of the …

This case report provides an overview of the current knowledge of the aetiology of AS, illustrates the pathway of surgical and non-surgical management of AS and provides a long-term review …

Nov 27, 2024 · Apert syndrome (AS) is a rare genetic disorder, which makes early diagnosis have a significant impact on prognosis and quality of life of patients. This syndrome often presents …

Feb 3, 2025 · Apert syndrome is a congenital condition characterized by coronal craniosynostosis, ex-orbitism, midface hypoplasia as well as symmetric syndactyly of both feet and hands. Apert …

Dec 18, 2024 · [Detección de una variante genética del Síndrome de Apert] Daniela Lynett 1, María Paola Lubo López 1, Laura Andrea Rojas Arbelaez 1, Paula Andrea Rodríguez Ocampo …

Apert syndrome is a developmental malformation characterized by craniosynostosis, a cone-shaped calvarium (acrocephaly), hypertelorism, midface hypoplasia, pseudo cleft-palate, a …

Jun 1, 2023 · Apert syndrome is an autosomal dominant inherited craniosynostosis syndrome. Males and females are equally affected. The incidence of the disease significantly increases …

Apert syndrome is one of the several genetic syndromes associated with craniosynostosis, a condition that includes premature fusion of one or multiple cranial sutures. There has been …