Comments about the article “A Crouzon syndrome from the classic period of Maya civilization?” The art historian’s point of view
Sign Up to like & getrecommendations! Published in 2019 at "Surgical and Radiologic Anatomy"
DOI: 10.1007/s00276-019-02302-y
Abstract: We read with great interest the article by Deps and Charlier, and entitled “A Crouzon syndrome from the classic period of Maya civilization?” [2]. We first would like to congratulate the authors for their valuable… read more here.
Keywords: period maya; civilization; period; classic period ... See more keywords
Lack of association of cranial lacunae with intracranial hypertension in children with Crouzon syndrome and Apert syndrome: a 3D morphometric quantitative analysis
Sign Up to like & getrecommendations! Published in 2019 at "Child's Nervous System"
DOI: 10.1007/s00381-019-04059-6
Abstract: PurposeCranial lacunae (foci of attenuated calvarial bone) are CT equivalents of “copper beating” seen on plain skull radiographs in children with craniosynostosis. The qualitative presence of copper beating has not been found to be useful… read more here.
Keywords: lacunae; intracranial hypertension; cranial lacunae; syndrome apert ... See more keywords
Sleep-related hypermotor epilepsy in a patient with mild Crouzon syndrome
Sign Up to like & getrecommendations! Published in 2017 at "Acta Neurologica Belgica"
DOI: 10.1007/s13760-017-0871-y
Abstract: Crouzon syndrome (CS) is a rare and complex autosomal dominant craniosynostosis with a highly variable phenotypic appearance and variable penetrance [1]. It was first described by French neurologist Octave Crouzon in 1912 [1]. The genetic… read more here.
Keywords: epilepsy; crouzon syndrome; hypermotor; sleep ... See more keywords
Pattern of Closure of Skull Base Synchondroses in Crouzon Syndrome.
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DOI: 10.1016/j.wneu.2017.09.208
Abstract: BACKGROUND The age of closure of skull base synchondroses has never been analyzed in a homogenous population of children with Crouzon syndrome. METHODS A retrospective case-control study was performed on 30 Crouzon children (17 male,… read more here.
Keywords: closure; closure skull; base synchondroses; crouzon syndrome ... See more keywords
Identification of Diagnostic Variants in FGFR2 and NPR2 Genes in a Chinese Family Affected by Crouzon Syndrome and Acromesomelic Dysplasia, Type Maroteaux.
Sign Up to like & getrecommendations! Published in 2022 at "DNA and cell biology"
DOI: 10.1089/dna.2022.0453
Abstract: This study aims to conduct a comprehensive clinical and genetic investigation on a large family with members having various phenotypes, including acromesomelic dysplasia, type Maroteaux (AMDM), idiopathic short stature (ISS), Crouzon syndrome (CS). Prenatal diagnosis… read more here.
Keywords: acromesomelic dysplasia; family; crouzon syndrome; dysplasia type ... See more keywords
An Infant with Crouzon Syndrome Presenting with Reversible Chronic Airway Obstruction.
Sign Up to like & getrecommendations! Published in 2020 at "Anesthesiology"
DOI: 10.1097/aln.0000000000003291
Abstract: Supplemental Digital Content is available in the text. read more here.
Keywords: infant crouzon; chronic airway; reversible chronic; crouzon syndrome ... See more keywords
Clinical assessment and FGFR2 mutation analysis in a Chinese family with Crouzon syndrome
Sign Up to like & getrecommendations! Published in 2021 at "Medicine"
DOI: 10.1097/md.0000000000024991
Abstract: Abstract Rationale: Crouzon syndrome is an autosomal dominant genetic disorder caused by mutations in fibroblast growth factor receptor 2 (FGFR2) and one of the most common types of craniosynostosis. Here we report the detection of… read more here.
Keywords: chinese family; crouzon syndrome; fgfr2 mutation; analysis ... See more keywords
Racial Disparity Between Asian and Caucasian Crouzon Syndrome in Skull Morphology.
Sign Up to like & getrecommendations! Published in 2020 at "Journal of Craniofacial Surgery"
DOI: 10.1097/scs.0000000000006741
Abstract: BACKGROUND Racial disparity in pathological consequences in skull growth may impact the treatment plan for different patient populations. This study attempts to explore the differences between Asian and Caucasian cranial morphology in Crouzon syndrome. METHOD… read more here.
Keywords: caucasian crouzon; crouzon; crouzon patients; crouzon syndrome ... See more keywords
Airway management in a patient with Crouzon syndrome proposed to orthognathic surgery
Sign Up to like & getrecommendations! Published in 2018 at "BMJ Case Reports"
DOI: 10.1136/bcr-2017-219371
Abstract: Airway management is one of the most important anaesthetist’s skills as major complications of airway management, although rare, can be among the most life threatening in medicine. Crouzon syndrome is a rare condition with physical… read more here.
Keywords: management; management patient; crouzon syndrome; airway management ... See more keywords
Patient with Crouzon Syndrome Treated with Modified Le Fort III Osteotomy without Previous Orthodontic Treatment: Case Report and a Review of the Literature
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DOI: 10.1155/2020/6248971
Abstract: Crouzon syndrome is the most common type of craniofacial dysostosis anomaly which presents a great challenge for clinicians since birth. Multiple synostoses in the sutures of the cranial base in this syndrome result in the… read more here.
Keywords: crouzon syndrome; case; patient crouzon; orthodontic treatment ... See more keywords
Crouzon’s Syndrome with a Dominant Sinus Pericranii Draining Transverse Sinus: Report of a Rare Association and Review of Literature
Sign Up to like & getrecommendations! Published in 2022 at "Pediatric Neurosurgery"
DOI: 10.1159/000524134
Abstract: Introduction: Crouzon’s syndrome and sinus pericranii (SP) are rare entities. Only few cases having both the features are reported. SP most commonly drains in relation to superior sagittal sinus and their communication to major posterior… read more here.
Keywords: sinus; sinus pericranii; crouzon syndrome; transverse sinus ... See more keywords