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 perspectives, ranging from surgical management to personal accounts.

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 variety of perspectives, ranging from surgical management to personal accounts.

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 present article is threefold: (1) to show the spectrum 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 of the dentofacial treatment outcomes.

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 respiratory and central nervous system complications.

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 syndrome is linked by autosomal dominant inheritance to fibroblast growth …

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 1, Lev Bladimir Ramirez 1, Daniel Jimenez 1, Luis Gustavo Celis Regalado 1, Nathalia Fonque Ojeda 1, Gabriela García Montoya 1. 1. Research Group on Cell Therapy and Metabolism, School of Medicine, Universidad de La Sabana ...

Apert syndrome is a developmental malformation characterized by craniosynostosis, a cone-shaped calvarium (acrocephaly), hypertelorism, midface hypoplasia, pseudo cleft-palate, a parrot beak-shaped nose, pharyngeal attenuation, and syndactyly of the hands and feet.

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 with paternal age and is felt to provide a selective advantage within the male spermatogonial cells.

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 significant clinical variation among different sutural synostoses and …