BOOK
Syndromes of the Head and Neck, An Issue of Atlas of the Oral & Maxillofacial Surgery Clinics, E-Book
(2014)
Additional Information
Book Details
Abstract
This issue of the Atlas of the Oral and Maxillofacial Surgery Clinics of North America serves as an aid to identification of 70 of the more important head and neck syndromes, and organized using the same nosology as in the landmark text of Robert Gorlin. As such, it should be useful to a varied audience, including not only the oral and maxillofacial surgeon but also the oral pathologist, the practitioner of oral medicine, and members of the craniofacial team--the orthodontist, pediatric dentist, speech and language specialist, geneticist, plastic surgeon, ENT specialist, pediatrician, nurse coordinator, and others. Areas covered include: Craniosynostosis Syndromes; Syndromes Affecting Bone; Metabolic and Autoimmune Syndromes; Syndromes Affecting Skin and Mucosa; Hamartoneoplastic Syndromes; Branchial Arch Syndromes; Clefting Syndromes; Syndromes Affecting the Central Nervous System; Chromosomal Syndromes; Syndromes with Unusual Facies; and Syndromes with Unusual Dental Findings or Gingival Components.
Table of Contents
| Section Title | Page | Action | Price |
|---|---|---|---|
| Front Cover | Cover | ||
| Syndromes of theHead and Neck\r | i | ||
| Copyright | ii | ||
| Contributors | iii | ||
| Contents | v | ||
| Atlas Of The Oral And Maxillofacial Surgery Clinics Of North America\r | viii | ||
| Dedication | ix | ||
| Preface\r | xi | ||
| Craniosynostosis Syndromes | 103 | ||
| Crouzon syndrome | 103 | ||
| Genetics | 103 | ||
| Clinical features | 103 | ||
| Differential diagnosis | 104 | ||
| Apert syndrome | 104 | ||
| Genetics | 104 | ||
| Clinical features | 104 | ||
| Syndromes Affecting Bone | 111 | ||
| Introduction | 111 | ||
| Osteopetrosis | 111 | ||
| Genetics | 111 | ||
| Clinical features | 111 | ||
| Differential diagnosis | 112 | ||
| Treatment considerations for the oral and maxillofacial surgeon | 112 | ||
| Osteopathia striata with cranial sclerosis | 113 | ||
| Genetic | 113 | ||
| Metabolic and Autoimmune Syndromes | 123 | ||
| Fabry disease | 123 | ||
| Genetics | 123 | ||
| Clinical features | 123 | ||
| Differential diagnosis | 123 | ||
| Syndromes Affecting Skin and Mucosa | 135 | ||
| Ehlers-Danlos syndromes | 135 | ||
| Clinical manifestations | 135 | ||
| Classic EDS (EDS I and EDS II) | 135 | ||
| Familial hypermobility EDS (EDS III) | 136 | ||
| Vascular (ecchymotic) EDS (EDS IV and EDS V) | 136 | ||
| EDS type VIII | 137 | ||
| Differential diagnosis | 137 | ||
| Treatment considerations for the oral and maxillofacial surgeon | 137 | ||
| Parry-Romberg syndrome | 137 | ||
| Clinical manifestations | 138 | ||
| Oral manifestations | 138 | ||
| Ophthalmologic manifestations | 138 | ||
| Neurologic manifestations | 138 | ||
| Differential diagnosis | 138 | ||
| Hamartoneoplastic Syndromes | 153 | ||
| Gorlin syndrome (nevoid basal cell carcinoma syndrome) | 153 | ||
| Gardner syndrome | 154 | ||
| Klippel-Trénaunay-Weber syndrome | 155 | ||
| Sturge-Weber syndrome | 156 | ||
| Peutz-Jeghers syndrome | 157 | ||
| Cowden syndrome | 158 | ||
| Multiple Endocrine Neoplasia syndromes | 159 | ||
| Proteus syndrome | 160 | ||
| Neurofibromatosis | 161 | ||
| Tuberous sclerosis | 162 | ||
| References | 164 | ||
| Branchial Arch Syndromes | 167 | ||
| Treacher Collins syndrome | 167 | ||
| Genetics (including inheritance patterns and frequency) | 167 | ||
| Clinical features | 167 | ||
| Treatment considerations for the oral and maxillofacial surgeon | 167 | ||
| Airway | 167 | ||
| Feeding | 167 | ||
| Hearing | 167 | ||
| Vision | 167 | ||
| Speech | 168 | ||
| Goldenhar syndrome | 168 | ||
| Genetics (including inheritance patterns and frequency) | 169 | ||
| Clinical features | 169 | ||
| Treatment considerations for the oral and maxillofacial surgeon | 170 | ||
| Möbius syndrome | 171 | ||
| Genetics (including inheritance patterns and frequency) | 171 | ||
| Clinical features | 172 | ||
| Treatment considerations for the oral and maxillofacial surgeon | 172 | ||
| Further readings | 172 | ||
| Clefting Syndromes | 175 | ||
| Introduction | 175 | ||
| Treatment considerations | 176 | ||
| Basic timeline for all cleft lip and palate disorders | 176 | ||
| Lip closure | 176 | ||
| Palate closure | 176 | ||
| Myringotomy | 176 | ||
| Pharyngeal flap | 177 | ||
| Rhinoplasty | 177 | ||
| Orthodontic care | 177 | ||
| Bone grafting | 177 | ||
| Orthognathic surgery | 177 | ||
| Distraction | 177 | ||
| Tooth replacement | 178 | ||
| Anesthesia | 178 | ||
| Compliance | 178 | ||
| Velocardiofacial syndrome (Shprintzen syndrome) | 178 | ||
| Genetics | 178 | ||
| Inheritance pattern | 178 | ||
| Frequency | 178 | ||
| Differential diagnosis | 178 | ||
| Treatment considerations for the oral and maxillofacial surgeon | 178 | ||
| Van Der Woude syndrome 1 and 2 | 179 | ||
| Syndromes Affecting the Central Nervous System | 183 | ||
| Lesch-Nyhan syndrome | 183 | ||
| Marcus Gunn syndrome | 184 | ||
| Cavernous sinus syndrome | 185 | ||
| Superior orbital fissure syndrome | 187 | ||
| Trotter syndrome | 187 | ||
| Horner syndrome | 188 | ||
| Frey syndrome | 190 | ||
| Ramsay-Hunt syndrome | 191 | ||
| Melkersson-Rosenthal syndrome | 192 | ||
| References | 193 | ||
| Chromosomal Syndromes | 197 | ||
| Down syndrome | 197 | ||
| Genetics | 197 | ||
| Clinical features | 197 | ||
| Differential diagnosis | 197 | ||
| Treatment considerations for the oral and maxillofacial surgeon | 198 | ||
| Klinefelter syndrome | 198 | ||
| Genetics | 198 | ||
| Clinical features | 198 | ||
| Differential diagnosis | 199 | ||
| Treatment considerations for the oral and maxillofacial surgeon | 199 | ||
| Turner syndrome | 200 | ||
| Genetics | 200 | ||
| Clinical features | 200 | ||
| Differential diagnosis | 201 | ||
| Treatment considerations for the oral and maxillofacial surgeon | 202 | ||
| References | 202 | ||
| Syndromes with Unusual Facies | 205 | ||
| Cornelia de Lange syndrome | 205 | ||
| Syndromes with Unusual Dental Findings or Gingival Components | 211 | ||
| Papillon-Lefevre syndrome | 211 | ||
| Genetics | 211 | ||
| Clinical features | 211 | ||
| Differential diagnosis | 211 | ||
| Treatment considerations | 211 | ||
| Hereditary gingival fibromatosis type 1 | 212 | ||
| Genetics | 212 | ||
| Clinical features | 212 | ||
| Differential diagnosis | 212 | ||
| Treatment considerations | 213 | ||
| Klippel-Feil syndrome | 213 | ||
| Genetics | 213 | ||
| Clinical features | 213 | ||
| Differential diagnosis | 213 | ||
| Treatment considerations | 214 | ||
| Oral-facial-digital syndrome type I | 214 | ||
| Genetics | 214 | ||
| Clinical features | 214 | ||
| Differential diagnosis | 215 | ||
| Treatment considerations | 215 | ||
| Oligodontia | 215 | ||
| Genetics | 215 | ||
| Clinical features | 216 |