Composite Frontal Bone Flap for Bony Reconstruction in Treacher Collins Syndrome and Hemifacial Microsomia

1987 ◽  
pp. 364-368
Author(s):  
Jacques M. Vaandrager
Keyword(s):  
Frontal Bone ◽  
Treacher Collins Syndrome ◽  
Bone Flap ◽  
Hemifacial Microsomia

Difficult Laryngoscopy/Intubation: The Child with Mandibular Hypoplasia

1983 ◽  
Vol 92 (4) ◽  
pp. 401-404 ◽  
Author(s):  
Steven D. Handler ◽  
Thomas P. Keon
Keyword(s):  
Temporomandibular Joint ◽  
Direct Laryngoscopy ◽  
Anterior Commissure ◽  
Difficult Laryngoscopy ◽  
Treacher Collins Syndrome ◽  
Pierre Robin Sequence ◽  
Hemifacial Microsomia ◽  
Mandibular Hypoplasia ◽  
Pierre Robin ◽  
Infants And Young Children

The child with mandibular hypoplasia (Treacher Collins syndrome, Pierre Robin sequence, hemifacial microsomia, etc) presents the otolaryngologist and anesthesiologist with considerable problems when direct laryngoscopy and/or endotracheal intubation is attempted. In addition to the small mandible, several other features of these patients contribute to the difficult laryngoscopy: macroglossia, glossoptosis, trismus related to temporomandibular joint abnormalities, and prominent maxilla or maxillary incisors. Most of the techniques that have been described for laryngoscopy/intubation in problem cases are difficult or impossible to use in infants and young children with mandibular hypoplasia. We present a modification of the standard direct laryngoscopic procedure, utilizing the 9-cm anterior commissure laryngoscope and an optical stylet in the task of exposing and intubating the larynx of a child with mandibular hypoplasia.

Reimplantation of Sterilized Autologous Frontal Bone Flap After Removal Because of Infection

1987 ◽  
pp. 479-480
Author(s):  
Hans Anderl ◽  
Wolfgang Mühlbauer ◽  
K. Twerdy
Keyword(s):  
Frontal Bone ◽  
Bone Flap

Use of a rivet-like titanium clamp closure system to replace an external frontal bone flap after transfrontal craniotomy in a dog

2005 ◽  
Vol 226 (5) ◽  
pp. 752-755 ◽  
Author(s):  
Peter N. Gordon ◽  
Joe N. Kornegay ◽  
Jimmy C. Lattimer ◽  
Cristi R. Cook ◽  
TerriAnn Tucker-Warhover
Keyword(s):  
Frontal Bone ◽  
Bone Flap ◽  
Closure System

scholarly journals Hemifacial Microsomia (HFM) and Treacher Collins Syndrome

2021 ◽  
pp. 1769-1812
Author(s):  
Manikandhan Ramanathan
Keyword(s):  
The Body ◽  
Treacher Collins Syndrome ◽  
Abnormal Development ◽  
Hemifacial Microsomia ◽  
Dentofacial Deformities ◽  
Dentofacial Deformity ◽  
Branchial Arches ◽  
Assessment And Treatment ◽  
Maxilla And Mandible ◽  
Parental Counselling

AbstractHemifacial microsomia and Treacher Collins syndrome are two entities which arise as a consequence of abnormal development of first and second branchial arches in utero. As a result, these dentofacial deformities present with abnormal facies especially the maxilla and mandible. They may also occur as part of other syndromes and may involve other structures of the body. In this chapter, we have discussed the etiology, clinical features, radiological assessment and treatment planning of such cases. Special emphasis should be made on early diagnosis, challenges of airway management and feeding and parental counselling. Since the two deformities are largely considered to be non-progressive, early distraction plays an important role in correction of the dentofacial deformity in these patients.

Ear Anomalies

2019 ◽  
pp. 63-68
Author(s):  
Robin D. Clark ◽  
Cynthia J. Curry
Keyword(s):  
Maternal Diabetes ◽  
Recurrence Risk ◽  
Treacher Collins Syndrome ◽  
Background Information ◽  
Hemifacial Microsomia ◽  
Mendelian Disorders ◽  
Organ Systems ◽  
Common Causes ◽  
Incidence Risk ◽  
Ear Anomalies

This chapter reviews background information about the incidence, risk factors, genetics, recurrence risk, family history and epidemiology of isolated and syndromic ear anomalies. The discussion on the differential diagnosis of ear anomalies summarizes its common causes, including teratogenic agents (isotretinoin, maternal diabetes, mycophenylate), chromosome anomalies (aneuploidy, 22q11 deletion), common sporadic multiple congenital anomaly syndromes (Hemifacial microsomia/Goldenhar), and Mendelian disorders that are primarily craniofacial (Treacher-Collins and other mandibulofacial dysostoses) and others that include malformations in other organ systems (CHARGE). The chapter gives recommendations for evaluation and management. A clinical case presentation features a child with mycophenylate embryopathy, who had been incorrectly diagnosed with Treacher Collins syndrome.

Maxillofacial prosthodontic management of a facial defect complicatedby a necrotic frontal bone flap: A clinical report

1999 ◽  
Vol 82 (1) ◽  
pp. 3-7 ◽  
Author(s):  
Ansgar C. Cheng ◽  
David Morrison ◽  
Alvin G. Wee ◽  
Walter G. Maxymiw ◽  
Daphne Archibald
Keyword(s):  
Frontal Bone ◽  
Bone Flap ◽  
Clinical Report ◽  
Facial Defect

Craniofacial surgery

2020 ◽  
pp. 289-314
Keyword(s):  
Vascular Malformations ◽  
Common Factor ◽  
Craniofacial Surgery ◽  
Treacher Collins Syndrome ◽  
Hemifacial Microsomia ◽  
The Face ◽  
The Common ◽  
Skull Deformity ◽  
The Uk ◽  
Single Suture

Craniofacial surgery is the subspecialist area of surgery that diagnoses and manages a large heterogeneous group of both congenital and acquired conditions. The common factor is the involvement of the cranium (and its contents) and the face. This chapter first introduces craniofacial surgery and goes on to cover craniosynostosis, single-suture synostosis, syndromic synostosis, torticollis and positional skull deformity, craniofacial procedures, craniofacial clefting disorders, tumours, vascular malformations of the head and neck, hemifacial microsomia, and Treacher Collins syndrome. Finally it outlines the members of the craniofacial team, and the organization of craniofacial services in the UK.

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