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Relevant bibliographies by topics / Craniofacial syndromes / Books

Books on the topic 'Craniofacial syndromes'

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Author: Grafiati

Published: 10 December 2022

Last updated: 29 January 2023

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1

B, Cassidy Suzanne, and Allanson Judith E, eds. Management of genetic syndromes. 2nd ed. Hoboken, N.J: Wiley-Liss, 2005.

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2

Yates, David M., and Michael R. Markiewicz, eds. Craniofacial Microsomia and Treacher Collins Syndrome. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-84733-3.

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3

Instrum, Susette M. Cephalometric comparison of the craniofacial skeletal morphology between mobius syndrome and non-syndromic controls. [Toronto: University of Toronto, Faculty of Dentistry], 1999.

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4

Instrum, Susette M. Craniofacial morphology and malocclusion in individuals with Mobius syndrome. [Toronto: University of Toronto, Faculty of Dentistry], 1998.

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5

Selnes, J. Eric. Cephalometric comparison of craniofacial morphology between velocardiofacial syndrome with confirmed 22q 11.2 microdeletions : isolated cleft palate and non-syndromic children. [Toronto: University of Toronto, Faculty of Dentistry], 1997.

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6

Parker, James N., and Philip M. Parker. Treacher Collins syndrome: A bibliography and dictionary for physicians, patients, and genome researchers [to Internet references]. San Diego, CA: ICON Health Publications, 2007.

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7

Management of Genetic Syndromes. 2nd ed. Wiley-Liss, 2004.

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8

Cassidy, Suzanne B., and Judith E. Allanson. Management of Genetic Syndromes. Wiley & Sons, Incorporated, John, 2010.

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9

Cassidy, Suzanne B., and Judith E. Allanson. Management of Genetic Syndromes. Wiley & Sons, Incorporated, John, 2005.

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10

Hopkins, Paul, and Laura Ryan. Difficult Airway. Edited by Erin S. Williams, Olutoyin A. Olutoye, Catherine P. Seipel, and Titilopemi A. O. Aina. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190678333.003.0015.

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The management of the difficult airway is one of the most challenging situations an anesthesiologist may encounter. The pediatric patient provides unique challenges such as lack of cooperation, rapid desaturation while apneic, and the presence of syndromes with craniofacial manifestations not frequently encountered in adults. These craniofacial manifestations may include mandibular hypoplasia, facial asymmetry, and limited mouth opening, to name a few. This chapter presents a case of a 5-year-old boy with Klippel-Feil syndrome and discusses the different aspects involved when dealing with a difficult airway in a pediatric patient, including the use of fiberoptic devices, neuromuscular blockade, and sedative premedication.

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11

Sobey, Christopher. Orofacial Pain. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190217518.003.0023.

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Management of orofacial pain in the general population can be a challenging and demanding undertaking due to the complex neurological anatomy and close proximity to vital structures. Differentiating various syndromes and origins of pain can prove difficult; thus, specific emphasis on establishing the correct diagnosis is of the utmost importance in formatting a successful treatment plan. The questions in this chapter delve into the presentations, physical exam findings, diagnostic testing, psychological effects, and evidence-based medical and interventional treatment algorithms of both common and less common craniofacial pain disorders. This chapter covers pathophysiology of the neurological, biomechanical, and central causes of facial pain.

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12

Howe, Peter. Craniosynostosis Repair. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199764495.003.0028.

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Craniosynostosis is a condition in which one or more of the fibrous sutures in an infant skull fuses prematurely. This may lead to restricted skull and brain growth and elevated intracranial pressure. Many children with craniosynostosis undergo corrective cranioplasty in infancy, an age when the skull is relatively large in proportion to the rest of the body. Depending on the operation, it is common for blood loss to be substantial and exceed the child's estimated blood volume (EBV). Managing this blood loss is challenging and requires careful planning for fluid and blood product administration. Some children also have craniofacial syndromes that are associated with airway obstruction and difficult intubation.

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13

Sabbe, Bryan M. General Anesthesia. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199398348.003.0023.

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This chapter covers various aspects of Pediatric General Anesthesia. Within this chapter topics covered include techniques for achieving induction of general anesthesia, along with limitations and potential complications of each. Also discussed is how to manage the pediatric airway, including mask ventilation, supraglottic airway devices, and endotracheal intubation, in addition to handling both expected and unexpected pediatric difficult airways. This includes assessment and airway management of several congenital craniofacial syndromes, and the means of achieving single-lung ventilation and lung separation in pediatric patients, along with evaluating and treating potential complications of each technique. Finally, means of defining, evaluating, and understanding the signs and stages of general anesthesia in pediatric patients are discussed.

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14

Meier, Petra M., and Thomas O. Erb. Craniosynostosis and Apert Syndrome. Edited by Kirk Lalwani, Ira Todd Cohen, Ellen Y. Choi, and Vidya T. Raman. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190685157.003.0021.

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Apert syndrome is a complex, progressive multisystem condition of the craniosynostosis spectrum originating from a fibroblast growth factor receptor disorder. Multidisciplinary treatment teams may include craniofacial surgery, neurosurgery, otolaryngology, ophthalmology, oro-maxillofacial surgery, and pediatric intensive care. Secondary to midface hypoplasia, children often present with a compromised airway and have a high incidence of sleep disorders. Anesthetic considerations include difficult airway assessment, the presence of obstructive sleep apnea syndrome, and increased intracranial pressure. Extensive remodeling procedures can be associated with massive hemorrhage (e.g., venous sinus bleeding) and venous air embolism. Transfusion-related complications include coagulopathy, metabolic derangements, and primarily noninfectious hazards such as transfusion-related acute lung injury and transfusion-related immunomodulation. Multimodal blood management should focus on a combination of appropriate surgical techniques and blood conservation, along with guidance from point-of-care testing (including coagulation).

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15

Yates, David, and Michael Markiewicz. Craniofacial Microsomia and Treacher Collins Syndrome: Comprehensive Treatment of Associated Facial Deformities. Springer International Publishing AG, 2021.

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16

Karen, Bellenir, ed. Congenital disorders sourcebook: Basic information about disorders acquired during gestation, including spina bifida, hydrocephalus, cerebral palsy, heart defects, craniofacial abnormalities, fetal alcohol syndrome, and more, along with current treatment options and statistical data. Detroit, MI: Omnigraphics, 1997.

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