[HTML][HTML] Unraveling the Complexity of Apert Syndrome: Genetics, Clinical Insights, and Future Frontiers
K Kumari, I Saleh, S Taslim, S Ahmad, I Hussain… - Cureus, 2023 - ncbi.nlm.nih.gov
Apert syndrome (AS), also known as type I acrocephalosyndactyly, is a rare congenital
condition characterized by craniosynostosis resulting from missense mutations in the …
condition characterized by craniosynostosis resulting from missense mutations in the …
Métodos de avaliação cognitiva de pacientes com Síndrome de Apert e de Crouzon
A Lovalho, A de Freitas Barreto, GHB Astolfi… - Medicina (Ribeirão …, 2023 - revistas.usp.br
Introdução: A Craniossinostose Coronal bilateral implica em diminuição do Perímetro
Craniano (PC) no eixo ântero-posterior (Braquicefalia) e frequentemente se associa ao …
Craniano (PC) no eixo ântero-posterior (Braquicefalia) e frequentemente se associa ao …
Subjective assessment of head and facial appearance in children with craniosynostoses after surgical treatment
D Larysz, E Nieroba - Healthcare, 2018 - mdpi.com
Background: Craniosynostoses are congenital defects in the construction of the skull
involving premature fusion of one or more cranial sutures. Premature fusion of sutures …
involving premature fusion of one or more cranial sutures. Premature fusion of sutures …
Craniosynostosis in a South Africa population
I Crous - 2021 - open.uct.ac.za
Background: Craniosynostosis refers to the premature fusion of calvarial bones which lead
to restricted growth potential. Compensatory growth occurs in the dimensions not restricted …
to restricted growth potential. Compensatory growth occurs in the dimensions not restricted …
[PDF][PDF] Apert syndrome in a Sri Lankan boy with normal head growth and without clinical features of raised intracranial pressure during infancy
M Manamperi, N Amarasinghe… - Sri Lanka Journal of …, 2023 - account.sljch.sljol.info
Apert syndrome is a rare syndrome with autosomal dominant inheritance affecting 1 in
65,000 newborns1, 2. It is a type of acrocephalosyndactyly characterized by …
65,000 newborns1, 2. It is a type of acrocephalosyndactyly characterized by …
[PDF][PDF] Cognitive assessment methods of patients with Apert and Crouzon syndrome
A de Freitas Lovalho, A de Freitas Barreto, GHB Astolfi… - revistas.usp.br
Introduction: Bilateral Coronal Craniosynostosis implies a decrease in the Cranial Perimeter
(CP) in the anteroposterior axis (Brachycephaly) and is frequently associated with an …
(CP) in the anteroposterior axis (Brachycephaly) and is frequently associated with an …
[PDF][PDF] Métodos de avaliação cognitiva de pacientes com Síndrome de Apert e de Crouzon
A de Freitas Lovalho, A de Freitas Barreto, GHB Astolfi… - repositorio.usp.br
Introdução: A Craniossinostose Coronal bilateral implica em diminuição do Perímetro
Craniano (PC) no eixo ânteroposterior (Braquicefalia) e frequentemente se associa ao …
Craniano (PC) no eixo ânteroposterior (Braquicefalia) e frequentemente se associa ao …