2021
DOI: 10.12691/ajmcr-9-4-2
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Crouzon’s Syndrome: A Case Report

Abstract: Crouzon's syndrome is a rare autosomal dominant disorder characterized by craniofacial malformations.It's the most common syndrome among the craniosynostosis group accounting for about 4.8 % of all of them. Crouzon syndrome is caused by mutation in the fibroblast growth factor receptor-2 (FGFR-2) gene resulting in premature closure of suture lines. Our article describes a case report of a 3 years old girl who displayed characteristic dysmorphic skull and facial features of Crouzon's syndrome.

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“…On radiographs, craniosynostosis can be seen as a copper-beaten appearance of the calvarium, which is brought on by irregular convolutional gyral patterning on the inner table of the calvarium as a result of the growing brain's continuous pulsatile pressure on the flexible cranium, which is best seen on the anterior aspect of the skull [ 3 ]. Crouzon's syndrome is among the various types of craniosynostosis, having a prevalence in the range of 15 to 16 cases per million live births [ 4 ]. This syndrome is usually associated with a triad of craniosynostosis, mid-face hypoplasia, and proptosis.…”
Section: Introductionmentioning
confidence: 99%
“…On radiographs, craniosynostosis can be seen as a copper-beaten appearance of the calvarium, which is brought on by irregular convolutional gyral patterning on the inner table of the calvarium as a result of the growing brain's continuous pulsatile pressure on the flexible cranium, which is best seen on the anterior aspect of the skull [ 3 ]. Crouzon's syndrome is among the various types of craniosynostosis, having a prevalence in the range of 15 to 16 cases per million live births [ 4 ]. This syndrome is usually associated with a triad of craniosynostosis, mid-face hypoplasia, and proptosis.…”
Section: Introductionmentioning
confidence: 99%