標(biāo)題: Titlebook: Craniofacial Microsomia and Treacher Collins Syndrome; Comprehensive Treatm David M. Yates,Michael R. Markiewicz Book 2022 Springer Nature [打印本頁] 作者: Gram114 時間: 2025-3-21 19:58
書目名稱Craniofacial Microsomia and Treacher Collins Syndrome影響因子(影響力)
書目名稱Craniofacial Microsomia and Treacher Collins Syndrome影響因子(影響力)學(xué)科排名
書目名稱Craniofacial Microsomia and Treacher Collins Syndrome網(wǎng)絡(luò)公開度
書目名稱Craniofacial Microsomia and Treacher Collins Syndrome網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Craniofacial Microsomia and Treacher Collins Syndrome被引頻次
書目名稱Craniofacial Microsomia and Treacher Collins Syndrome被引頻次學(xué)科排名
書目名稱Craniofacial Microsomia and Treacher Collins Syndrome年度引用
書目名稱Craniofacial Microsomia and Treacher Collins Syndrome年度引用學(xué)科排名
書目名稱Craniofacial Microsomia and Treacher Collins Syndrome讀者反饋
書目名稱Craniofacial Microsomia and Treacher Collins Syndrome讀者反饋學(xué)科排名
作者: Jingoism 時間: 2025-3-21 20:57
Etiology and Anatomical Variance in Craniofacial Microsomiations for children with CFM. CFM has a variable presentation which can range from mild preauricular skin tags to bilateral complete agenesis of structures. This variability and its influence on surgical interventions will be examined.作者: 憂傷 時間: 2025-3-22 04:14 作者: FRAUD 時間: 2025-3-22 07:43 作者: municipality 時間: 2025-3-22 11:05 作者: Pastry 時間: 2025-3-22 13:55 作者: Pastry 時間: 2025-3-22 19:17
Associated Systemic Health Conditions Associated with Treacher Collins Syndromegastrointestinal system, and genitourinary system. We will also be reviewing how the patient’s dental health and psychiatric health will be affected. The goal of this chapter is to broaden the focus of the treatment of Treacher Collins to create a more holistic understanding of this syndrome.作者: AUGER 時間: 2025-3-22 23:56 作者: 輕彈 時間: 2025-3-23 02:20 作者: Watemelon 時間: 2025-3-23 09:04
eating these children.Written by experts in the fieldThe book provides a framework for diagnosis and treatment of the complex facial deformities found in craniofacial microsomia and Treacher Collins syndrome. These conditions are difficult to treat due to their complexity and variable presentation. 作者: Leisureliness 時間: 2025-3-23 09:51
Warum sollte die Welt Gesetzen folgen?,tions for children with CFM. CFM has a variable presentation which can range from mild preauricular skin tags to bilateral complete agenesis of structures. This variability and its influence on surgical interventions will be examined.作者: capsule 時間: 2025-3-23 17:32 作者: 假設(shè) 時間: 2025-3-23 18:12 作者: glucagon 時間: 2025-3-24 00:48
https://doi.org/10.1007/978-3-540-49491-1ssues, creating an articulation between the mandible and the temporal bone when missing, promoting maxillary growth, and establishing a functional occlusion and esthetic appearance of the face and dentition. Treatment concepts for the growing child with CFM will be discussed.作者: defeatist 時間: 2025-3-24 02:40
Theorien als Strukturen I: Kuhns Paradigmen,rioritizing life and limb, in this case airway and ocular structures, and supporting vital functions, such as respiration, hearing, and nutrition. Comprehensive treatment is best accomplished by a multidisciplinary team.作者: 后天習(xí)得 時間: 2025-3-24 09:38
The Core Functions of MediaWikigastrointestinal system, and genitourinary system. We will also be reviewing how the patient’s dental health and psychiatric health will be affected. The goal of this chapter is to broaden the focus of the treatment of Treacher Collins to create a more holistic understanding of this syndrome.作者: muster 時間: 2025-3-24 11:01 作者: arrogant 時間: 2025-3-24 16:30 作者: 一起 時間: 2025-3-24 20:36
A Look at Breathing, Feeding/Swallowing, and Speech Impairment in Patients with Craniofacial Microsother extra craniofacial malformations that can impact breathing, feeding/swallowing, and speech/language development. This chapter will review normal swallowing and speech development and highlight the challenges that can be associated with CFM such as obstructive sleep apnea, dysphagia, hearing loss, and speech and language delays.作者: Champion 時間: 2025-3-25 02:48
Microtia Reconstruction in Patients with Craniofacial Microsomiaapter is to provide protocols for the three most common techniques with pearls for obtaining optimal results. The advantages and disadvantages of three reconstructive approaches will be addressed to support shared decision-making among surgeons, anaplastologists, psychologists, patients, and their families.作者: Functional 時間: 2025-3-25 04:29
Warum sollte die Welt Gesetzen folgen?,ther extra craniofacial malformations that can impact breathing, feeding/swallowing, and speech/language development. This chapter will review normal swallowing and speech development and highlight the challenges that can be associated with CFM such as obstructive sleep apnea, dysphagia, hearing loss, and speech and language delays.作者: Nefarious 時間: 2025-3-25 09:39
Warum sollte die Welt Gesetzen folgen?,apter is to provide protocols for the three most common techniques with pearls for obtaining optimal results. The advantages and disadvantages of three reconstructive approaches will be addressed to support shared decision-making among surgeons, anaplastologists, psychologists, patients, and their families.作者: 果仁 時間: 2025-3-25 12:22
David M. Yates,Michael R. MarkiewiczProvides a comprehensive approach in treating this complex patient population.Provides the reader with literature based best practices in treating these children.Written by experts in the field作者: 說明 時間: 2025-3-25 16:10
http://image.papertrans.cn/c/image/239287.jpg作者: 虛度 時間: 2025-3-25 21:47
Warum sollte die Welt Gesetzen folgen?,This introductory chapter provides a concise background on Treacher Collins syndrome, its genetic origins, its embryological origins from the cranial neural crest and the neurocristopathy leading to its characteristic craniofacial malformations, and its anatomical and morphological defects.作者: 犬儒主義者 時間: 2025-3-26 00:32
Theorien als Strukturen I: Kuhns Paradigmen,In this chapter, we discuss the roles of the speech and language pathologist and otolaryngologist as members of the craniofacial team when managing patients with Treacher Collins syndrome.作者: 中國紀(jì)念碑 時間: 2025-3-26 04:26
Etiology and Anatomical Variation in Treacher Collins SyndromeThis introductory chapter provides a concise background on Treacher Collins syndrome, its genetic origins, its embryological origins from the cranial neural crest and the neurocristopathy leading to its characteristic craniofacial malformations, and its anatomical and morphological defects.作者: MEAN 時間: 2025-3-26 10:10 作者: 網(wǎng)絡(luò)添麻煩 時間: 2025-3-26 12:48
https://doi.org/10.1007/978-3-030-84733-3Facial Anomalies; Facial Deformities; Orthodontic Considerations; MaxilloMandibular Deformities; Orbital作者: 似少年 時間: 2025-3-26 18:58 作者: 指耕作 時間: 2025-3-26 23:03
Warum sollte die Welt Gesetzen folgen?,The various beliefs will be presented in this chapter. There are two main classification systems for CFM which are used to diagnose and guide interventions for children with CFM. CFM has a variable presentation which can range from mild preauricular skin tags to bilateral complete agenesis of struct作者: Ruptured-Disk 時間: 2025-3-27 01:28 作者: SUE 時間: 2025-3-27 06:07
Warum sollte die Welt Gesetzen folgen?,ther extra craniofacial malformations that can impact breathing, feeding/swallowing, and speech/language development. This chapter will review normal swallowing and speech development and highlight the challenges that can be associated with CFM such as obstructive sleep apnea, dysphagia, hearing los作者: EWER 時間: 2025-3-27 10:22
Warum sollte die Welt Gesetzen folgen?,t congenital differences involving at least one other organ system, including vertebral, cardiac, central nervous, developmental, genitourinary, gastrointestinal, and pulmonary. This chapter provides an overview of the extracraniofacial systems that may be involved, associated diagnoses, physical ex作者: 拍翅 時間: 2025-3-27 14:18
https://doi.org/10.1007/978-3-540-49491-1hetics at completion of craniofacial growth. Treatment is directed toward increasing the size of the underdeveloped and malformed mandible and soft tissues, creating an articulation between the mandible and the temporal bone when missing, promoting maxillary growth, and establishing a functional occ作者: 信徒 時間: 2025-3-27 20:53
Die Grenzen des Falsifikationismus,tition, and occlusion with extreme variability of expression which can include severe hypoplasia or absence of the TMJ, presenting a major reconstruction challenge to optimally correct the functional and esthetic deformities. For the more severe cases, surgical correction will commonly include TMJ r作者: TEM 時間: 2025-3-27 22:51 作者: 波動 時間: 2025-3-28 03:29
Warum sollte die Welt Gesetzen folgen?,e bilateral. The deviating growth is characterized by asymmetry and a retrognathic or even micrognathic mandible. The mandibular growth pattern is characterized by a clockwise rotation. Delayed dental eruption and hypodontia on the affected side and midline shifting are expected, with an increased c作者: gangrene 時間: 2025-3-28 07:01
Die Grenzen des Falsifikationismus, are occasionally observed in TCS but are rare in HFMS. Hearing loss in TCS is largely bilateral, whereas hearing loss is generally asymmetric or unilateral in HFMS. In both syndromes, the hearing loss is largely conductive in nature, but some patients also have a mixed hearing loss. Sensorineural h作者: 明智的人 時間: 2025-3-28 13:17 作者: CLEAR 時間: 2025-3-28 16:37 作者: left-ventricle 時間: 2025-3-28 22:08
Warum sollte die Welt Gesetzen folgen?,ble, dentition and occlusion, orbits, ears, muscles, nerves, and soft tissues of the head and neck region with secondary psychosocial and behavioral issues, as well as disturbances in speech, breathing, and sleep impairment. A variety of treatment options exist with personal surgeon preferences and 作者: Ambulatory 時間: 2025-3-28 23:25 作者: BAN 時間: 2025-3-29 04:02 作者: tangle 時間: 2025-3-29 08:20
The Core Functions of MediaWiki at birth that facilitate a clinical diagnosis. The periorbital abnormalities are a hallmark of the syndrome and are considered to be skeletal and soft tissue expressions of Tessier clefts 6, 7, and 8. Notable features include lateral orbital rim hypoplasia, orbital volume deficiency, lateral lower 作者: Mediocre 時間: 2025-3-29 11:50
Etiology and Anatomical Variance in Craniofacial MicrosomiaThe various beliefs will be presented in this chapter. There are two main classification systems for CFM which are used to diagnose and guide interventions for children with CFM. CFM has a variable presentation which can range from mild preauricular skin tags to bilateral complete agenesis of struct作者: 藕床生厭倦 時間: 2025-3-29 17:52
Initial Evaluation of a Patient with Craniofacial Microsomiafrom the first and second branchial arches. Within this spectrum there is a significant phenotypic variability with the most commonly affected structures being the external ear, middle ear, mandible, temporomandibular joint, muscles of mastication, and muscles of facial expression. This chapter comp作者: 名詞 時間: 2025-3-29 21:32 作者: comely 時間: 2025-3-30 00:47 作者: 勤勉 時間: 2025-3-30 07:35 作者: 過時 時間: 2025-3-30 08:40 作者: 捏造 時間: 2025-3-30 14:26
Definitive Reconstruction of Associated Maxillomandibular Deformities in Craniofacial Microsomia a growing number of patients receive a costochondral graft to reconstruct a temporomandibular joint, and that is able to adequately position the maxillomandibular complex, all the patients may need further orthodontic treatment. In that case, the growing number of patients received a definitive tre作者: organism 時間: 2025-3-30 19:13
Orthodontic Considerations in the Craniofacial Microsomia Patientse bilateral. The deviating growth is characterized by asymmetry and a retrognathic or even micrognathic mandible. The mandibular growth pattern is characterized by a clockwise rotation. Delayed dental eruption and hypodontia on the affected side and midline shifting are expected, with an increased c作者: FLOUR 時間: 2025-3-30 21:33 作者: pus840 時間: 2025-3-31 03:15 作者: 自然環(huán)境 時間: 2025-3-31 07:23
Correction of the Soft Tissue Deformities Associated with Craniofacial Microsomia: Facial Reanimatiothe first and second branchial arches. The degree of involvement is very variable. The SAT and OMENS classification systems incorporate soft tissue in their schemes. The extent of soft tissue deficiency is related to the severity of the mandible deformity. Soft tissue structures that can be affected作者: POINT 時間: 2025-3-31 10:06
An Overview of Treatment and Recommendations for the Craniofacial Microsomia Patientble, dentition and occlusion, orbits, ears, muscles, nerves, and soft tissues of the head and neck region with secondary psychosocial and behavioral issues, as well as disturbances in speech, breathing, and sleep impairment. A variety of treatment options exist with personal surgeon preferences and 作者: 碌碌之人 時間: 2025-3-31 15:50
Initial Evaluation of a Patient with Treacher Collins Syndrome jaw bones. The initial assessment of a patient with TCS is one of the most important steps to address a patient’s needs in a coherent fashion while prioritizing life and limb, in this case airway and ocular structures, and supporting vital functions, such as respiration, hearing, and nutrition. Com
