Results 1 to 10 of about 5,138 (198)

Clues from Crouzon: Insights into the potential role of growth factors in the pathogenesis of myelinated retinal nerve fibers [PDF]

Journal of Current Ophthalmology, 2016
Purpose: We present a case of bilateral extensive peripapillary myelinated retinal nerve fibers (MRNF) in an individual with Crouzon syndrome, an inherited form of craniosynostosis caused by overactivation of fibroblast growth factor receptor 2.
Giancarlo A. Garcia, Jack J. Tian, Supanut Apinyawasisuk, Sarah Kim, Handan Akil, Alfredo A. Sadun   +5 more
doaj   +5 more sources

Familial Crouzon syndrome

Contemporary Clinical Dentistry, 2010
Crouzon syndrome is an autosomal dominant condition of the craniosynostotic syndromes without syndactyly and with various dentofacial anomalies.
Y Samatha, T Harsha Vardhan, A Ravi Kiran, A J Sai Sankar, B Ramakrishna   +4 more
doaj   +3 more sources

Crouzon syndrome

Medical Journal of Dr. D.Y. Patil University, 2013
Crouzon syndrome is an autosomal dominant disorder with complete penetrance and variable expressivity. Described by a French neurosurgeon in 1912, it is a rare genetic disorder.
Neha Rajappa, Sadananda Patra, Abha Gahlot, Snehal Bhalsing   +3 more
doaj   +2 more sources

CROUZON SYNDROME

Delhi Journal of Ophthalmology, 2010
A 27 year old male patient presented with sudden onset of pain, redness, photophobia and diminution of vision in left eye since 10 days, no past history of ocular injury. At presentation visual acuity in right eye was 6/9 and that of left eye was HM +ve,
Navin Chandra
doaj   +3 more sources

Crouzon Syndrome

Citation: 'Crouzon syndrome' in the IUPAC Compendium of Chemical Terminology, 5th ed.; International Union of Pure and Applied Chemistry; 2025. Online version 5.0.0, 2025. 10.1351/goldbook.10575 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
Zeppieri M, Karsonovich T, Patel BC.
europepmc   +2 more sources

Generation of human induced pluripotent stem cell lines from patients with FGFR2-linked syndromic craniosynostosis [PDF]

Disease Models & Mechanisms
Max Gijsbertsen, Irene M. J. Mathijssen, Ana F. Duarte Madancos, Johannes P. T. M. van Leeuwen, Jeroen van de Peppel   +4 more
doaj   +2 more sources

Unexpected massive bleeding during the modified LeFort III advancement surgery for Crouzon syndrome: A case report [PDF]

Clinical Case Reports
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 ...
Zahra Sadat Modarresi, Narges Hajiani, Zeinab Bakhtiari, Farnoush Mohammadi   +3 more
doaj   +2 more sources

QS3: Influence Of Nonsyndromic Bicoronal Synostosis And Syndromic Influences On And Periorbital Malformation

Plastic and Reconstructive Surgery, Global Open, 2021
Background Oculo-orbital disproportion in patients with craniosynostosis have similarities and dissimilarities between syndromic and nonsyndromic cases. We hypothesize these two conditions have specific individual influences as it relates to development ...
Xiaona Lu, MD, PhD, Antonio Jorge Forte, MD, PhD, Michael Alperovich, MD, Nivaldo Alonso, MD, PhD, John A. Persing, MD   +4 more
doaj   +1 more source

Crouzon syndrome with acanthosis nigricans: A case report and literature review

Dermatology Reports, 2022
Crouzon’s syndrome with acanthosis nigricans is an autosomal dominant disease, with typical features of classic Crouzon craniosynostosis, verrucous hyperplasia, and hyperpigmentation of the skin.
Quan Duy Nguyen, Tu Nguyen Anh Tran, Hao Trong Nguyen   +2 more
doaj   +1 more source

Crouzon syndrome and the eye: An overview

Indian Journal of Ophthalmology, 2022
The current literature review aims to evaluate the ocular findings and associated ophthalmic features in Crouzon syndrome. Craniosynostoses are syndromes characterized by premature fusion of sutures of the skull and Crouzon syndrome is the most common of
Kasturi Bhattacharjee, Obaidur Rehman, Vatsalya Venkatraman, Don Kikkawa, Harsha Bhattacharjee, Rahul Gogoi, Aditi Mehta Grewal, Pragya Bhattacharjee   +7 more
doaj   +1 more source