Zobrazeno 1 - 10
of 1 858
pro vyhledávání: '"crouzon syndrome"'
Publikováno v:
Clinical Case Reports, Vol 12, Iss 7, Pp n/a-n/a (2024)
Key Clinical Message Vigilant monitoring for postoperative complications, including bleeding and dysrhythmia, is crucial in patients with craniosynostosis syndromes like Crouzon syndrome undergoing craniofacial surgery, with a thorough evaluation, in
Externí odkaz:
https://doaj.org/article/61a300362a114a0ba9cd07892660f805
Autor:
Neeharika P Shah, Omkar N Gadre
Publikováno v:
TNOA Journal of Ophthalmic Science and Research, Vol 62, Iss 1, Pp 117-120 (2024)
Craniosynostoses are syndromes characterized by premature fusion of sutures of the skull and Crouzon syndrome is the most common of the craniosynostosis syndromes. Early fusion of sutures causes craniofacial anomalies. Visual complications can arise-
Externí odkaz:
https://doaj.org/article/f20bb0d8e4234636aa87645e8658b89a
Autor:
Zarzycki, Jenna, Peté, Sara
Publikováno v:
Alki: The Washington Library Association Journal. Jul2022, Vol. 38 Issue 2, p46-49. 2p.
Publikováno v:
Journal of Plastic and Reconstructive Surgery, Vol 2, Iss 3, Pp 102-106 (2023)
A human tail complicated by Crouzon syndrome is extremely rare, with only eight reported cases of human tails associated with Crouzon syndrome. A human tail is defined as a true human tail or a pseudo-human tail according to the presence or absence o
Externí odkaz:
https://doaj.org/article/f5707604d0f648328795dc47060d47a4
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 32, Iss , Pp 101904- (2023)
Purpose: We present a case of a 10-year-old boy with Crouzon syndrome that demonstrates progressive myelinated retinal nerve fibers (MRNF). Observations: A 10-year-old boy was referred for ophthalmic examination due to clusters of opaque white fibers
Externí odkaz:
https://doaj.org/article/729ec318cb7144e692ff854fa75998be
Publikováno v:
International Journal of Medical Arts, Vol 5, Iss 3, Pp 3133-3136 (2023)
Background: Hydrocephalous in the presence of primary craniosynostosis is a unique condition with respect to pathogenesis, clinical significance, and morphological appearance. It is rarely observed in nonsyndromic craniosynostosis, and in these cases
Externí odkaz:
https://doaj.org/article/09d505477bb445f78ef7046af2de6dcc
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-7 (2023)
Abstract Background Crouzon syndrome, a rare genetic disorder characterized by premature closure of coronal sutures, results in skull and facial deformities along with abnormal brain and ocular development. Case presentation Here, we report a case of
Externí odkaz:
https://doaj.org/article/d477a6a7e6094074a924feb979a000e4
Publikováno v:
Archives of Plastic Surgery, Vol 50, Iss 01, Pp 054-058 (2023)
Patients with Crouzon syndrome have increased risks of cerebrospinal fluid rhinorrhea and meningoencephalocele after LeFort III osteotomy. We report a rare case of meningoencephalocele following LeFort III midface advancement in a patient with Crouzo
Externí odkaz:
https://doaj.org/article/5827fc47c4cf46819b4a1e8c285b882f
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