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The Anatomical Record, Volume 308, Issue 7, Page 1944-1971, July 2025.Abstract Craniosynostosis is a common yet complex birth defect, characterized by premature fusion of the cranial sutures that can be syndromic or nonsyndromic. With over 180 syndromic associations, reaching genetic diagnoses and understanding variations in underlying cellular mechanisms remains a challenge.
Heather A. Richbourg +9 more
wiley +1 more source
Oral manifestations of Crouzon Syndrome and their implications for dental care: case report [PDF]
RGO: Revista Gaúcha de OdontologiaCrouzon Syndrome is a rare genetic disease that affects craniofacial development resulting in various manifestations in the head and neck region. This article aimed to report a clinical case of a patient with Crouzon Syndrome, highlighting the relevant ...
Ana Paula Otoni Sena +5 more
doaj +1 more source
Fibroblast growth factor signaling in skeletal development and disease [PDF]
, 2015 Fibroblast growth factor (FGF) signaling pathways are essential regulators of vertebrate skeletal development. FGF signaling regulates development of the limb bud and formation of the mesenchymal condensation and has key roles in regulating ...
Marie, Pierre J, Ornitz, David M
core +2 more sources
Premature Craniosynostosis in a Rare Genetic Disease- A Case Report
Iranian Journal of Public Health, 2015 Background: Crouzon syndrome is a rare genetic disorder inherited in autosomal dominant pattern with complete penetration and variable expressivity.Its most notable characteristic feature is premature synostosis of cranial sutures .The case presented is ...
Hasnain Abbas Dharamshi +6 more
doaj
Crouzon Syndrome: Clinical case
Педиатрическая фармакология, 2019 Relevance. Crouzon syndrome is a craniostenosis due to combination of cranial bones hypoplasia and premature ectocranial sutures fusion resulting in deformation of cerebral and facial cranium.
Nikolai I. Zryachkin +3 more
doaj +1 more source
General and oral aspects in Apert syndrome: report of a case [PDF]
, 2015 Background: The present paper describes the general and oral manifestations in a 32-year-old man previously diagnosed with Apert syndrome. Clinical examination revealed features of acrocephalosyndactyly.
Chimenos Küstner, Eduardo +5 more
core +1 more source
Obstructive sleep apnea in children [PDF]
, 2010 Childhood obstructive sleep apnea syndrome (OSAS) is characterized by recurrent episodes of partial or complete upper airway obstruction during sleep.
Fagondes, Simone Chaves +1 more
core +3 more sources
Prosthetic rehabilitation of a Crouzon patient: A case report
Contemporary Clinical Dentistry, 2010 Crouzon syndrome is a rare genetic disorder, which can be defined as a variation of craniofacial dysostosis caused by the premature obliteration and ossification of two or more sutures.
Hanefi Kurt +2 more
doaj +1 more source
Sensory perception in preschool children affected by autism spectrum disorder: A pilot study [PDF]
, 2017 Introduction: Autism spectrum disorder (ASD) is a behavioral syndrome caused by a developmental disorder, biologically determined, with onset in the first three years of life.
Di Filippo, T +6 more
core +1 more source
EMotional Intelligence And Obstructive Sleep Apnea Syndrome In Children: Preliminary Case-Control Study [PDF]
, 2017 Introduction: Obstructive sleep apnea syndrome (OSAS) affects up to 4% of pediatric population, with many co-morbidities in the medium-long term. Functional alterations in prefrontal cortex (PFC) may explain why OSAS impacts aspects such as: executive ...
DI FILIPPO, T. +8 more
core +1 more source