Crouzon\'s Syndrome: A Rare Genetic Disorder
Author:
Publisher
Jaypee Brothers Medical Publishing
Subject
Periodontics,Oral Surgery,Pediatrics, Perinatology and Child Health,Orthodontics
Link
https://www.ijcpd.com/doi/pdf/10.5005/jp-journals-10005-1395
Reference14 articles.
1. 1. Helms JA, Schneider RA. Cranial skeletal biology. Nature 2003 May;423(6937):326-331.
2. 2. Crouzon LE. Dysostose cranio-faciale héréditaire. Bulletin de la Société des Médecins des Hôpitaux de Paris 1912;33:545-555.
3. 3. Fries PD, Katowitz JA. Congenital craniofacial anomalies of ophthalmic importance. Surv Ophthalmol 1990 Sep- Oct;35(2):87-119.
4. 4. Hlongwa P. Early orthodontic management of Crouzon syndrome: a case report. J Maxillofac Oral Surg 2009 Mar;8(1): 74-76.
5. 5. Kreiborg S. Crouzon syndrome. Scand J Plast Reconstr Surg 1981;18(Suppl):1-198.
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1. Crouzon Syndrome Spanning Three Generations: Advances in the Treatment of Syndromic Midface Deficiency;Plastic and Reconstructive Surgery - Global Open;2023-11
2. Mysterious Bilateral Foot Pain in a Child With Crouzon Syndrome;Cureus;2023-04-01
3. ORDENTAL MANIFESTATIONS OF CRUZON SYNDROME (Clinical case);Actual problems in dentistry;2022-02-04
4. Rare Genetic Syndromes and Oral Anomalies: A Review of the Literature and Case Series with a New Classification Proposal;Children;2021-12-26
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