Management of obstructive sleep apnea in a Treacher Collins syndrome patient using distraction osteogenesis of the mandible

Damlar, İbrahim; Altan, Ahmet; Turgay, Berk; Kılıç, Soydan

doi:10.5125/jkaoms.2016.42.6.388

Cited by 7 publications

(6 citation statements)

References 17 publications

(28 reference statements)

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“…ENT detailed examination is required for identification of important components for future treatment interventions (Plomp et al, 2015 ). In many cases the orthognathic correction, like the mandibular DO increases the airway and prevents the OSAS (Damlar et al, 2016 ). Articulatory dysfunction should be improved or corrected for proper social integration and quality of life of these children (Golinko et al, 2016 ).…”

Section: Discussionmentioning

confidence: 99%

Update on 13 Syndromes Affecting Craniofacial and Dental Structures

Bartzela¹,

Carels²,

Maltha³

2017

Front. Physiol.

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Care of individuals with syndromes affecting craniofacial and dental structures are mostly treated by an interdisciplinary team from early childhood on. In addition to medical and dental specialists that have a vivid interest in these syndromes and for whom these syndromes are of evident interest, experts of scientific background—like molecular and developmental geneticists, but also computational biologists and bioinformaticians—, become more frequently involved in the refined diagnostic and etiological processes of these patients. Early diagnosis is often crucial for the effective treatment of functional and developmental aspects. However, not all syndromes can be clinically identified early, especially in cases of absence of known family history. Moreover, the treatment of these patients is often complicated because of insufficient medical knowledge, and because of the dental and craniofacial developmental variations. The role of the team is crucial for the prevention, proper function, and craniofacial development which is often combined with orthognathic surgery. Although the existing literature does not provide considerable insight into this topic, this descriptive review aims to provide tools for the interdisciplinary team by giving an update on the genetics and general features, and the oral and craniofacial manifestations for early diagnosis. Clinical phenotyping together with genetic data and pathway information will ultimately pave the way for preventive strategies and therapeutic options in the future. This will improve the prognosis for better functional and aesthetic outcome for these patients and lead to a better quality of life, not only for the patients themselves but also for their families. The aim of this review is to promote interdisciplinary interaction and mutual understanding among all specialists involved in the diagnosis and therapeutic guidance of patients with these syndromal conditions in order to provide optimal personalized care in an integrated approach.

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Section: Discussionmentioning

confidence: 99%

Update on 13 Syndromes Affecting Craniofacial and Dental Structures

Bartzela¹,

Carels²,

Maltha³

2017

Front. Physiol.

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“…Based on our own treatment experience and referring to the treatment of other researchers, [10][11][12][13][14] we have summarized the comprehensive serial treatment of TCS, which is mainly formulated based on patient age and deformity assessment for clinical reference (Supplemental Table 1, Supplemental Digital Content 4, http://links.lww.com/SCS/E179).…”

Section: Discussionmentioning

confidence: 99%

Comprehensive Serial Treatment of Treacher Collins Syndrome

Lei¹,

Huang²,

Sun³

et al. 2022

Journal of Craniofacial Surgery

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Objective: To discuss and summarize the comprehensive serial surgical treatment of Treacher Collins syndrome. Materials and Methods: From September 2012 to January 2020, 12 patients with Treacher Collins syndrome were treated by autologous fat graft, mandibular distraction osteogenesis, orbitozygomatic reconstruction with calvarial external lamina, orthognathic surgery combined with postoperative orthodontics, transplantation of upper eyelid orbicularis myocutaneous flap, lateral canthal ligament reduction, and other methods. The authors evaluated the postoperative improvement, summarized experiences, and reviewed literatures about the comprehensive serial treatment of Treacher Collins syndrome. Results: All patients showed significant improvement in appearance and function, and no complications were found during the follow-up period of 5 months to 3 years. Conclusions: The deformities of Treacher Collins syndrome involves multiple craniofacial region, and only by formulating comprehensive serial treatment strategies according to the malformation characteristics of different patients can the best effect be achieved.

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“…37 Bu dönemde Lefort 1 ve çift tarafl ı sagital split osteotomisi ile ileri dönem okluzal düzlem problemleri çözülebilir. 41 Damlar ve ark., 42 tarafından bildirilen vakada 10 yaşındaki TCS' li kız hastada mandibular ve maksiller hipoplazisi saptanmıştır. Radyografik muayene sonrası mandibula distraksiyon osteogenezisi planlanmış olup, hastanın uyku apnesi şikayetinden kurtularak hava yolu açıklığının arttırılması sağlanmıştır.…”

Section: Faz III Tedaviunclassified

“…37 Bu dönemde Lefort 1 ve çift tarafl ı sagital split osteotomisi ile ileri dönem okluzal düzlem problemleri çözülebilir. 41 Damlar ve ark., 42…”

Section: Introductionunclassified

Treacher Collins Sendromu’nda Dentofasiyal Bulgular ve Tedavi Yaklaşımı

Soğukpınar

Mutluay²

2019

Sakarya Medical Journal

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DERLEME / Review Öz Treacher Collins Sendromu (TCS); kafatası ve yüzdeki bozukluklar ile karakterize genetik bir rahatsızlıktır. Literatürde bu sendroma sahip hastaların ağız içi bulguları; açık kapanış, çapraşıklık, diş agenezi, mine opasiteleri, ektopik erüpsiyonlar, makrodonti ve periodontal problemler olarak rapor edilmektedir. TCS'li hastaların tedavisinde; erken teşhisle birlikte aralarında çocuk diş hekimi ve ortodontistin bulunduğu multidisipliner bir ekibin yaklaşım gerekmektedir. Bu derlemede; TCS'nin genetik ve sitogenetik özellikleri ile sistemik ve dental tedavi ihtiyaçları ele alınmaktadır.

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Management of obstructive sleep apnea in a Treacher Collins syndrome patient using distraction osteogenesis of the mandible

Cited by 7 publications

References 17 publications

Update on 13 Syndromes Affecting Craniofacial and Dental Structures

Update on 13 Syndromes Affecting Craniofacial and Dental Structures

Comprehensive Serial Treatment of Treacher Collins Syndrome

Treacher Collins Sendromu’nda Dentofasiyal Bulgular ve Tedavi Yaklaşımı

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