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Oxford Handbook of Clinical Dentistry$
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Laura Mitchell, David A. Mitchell

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Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct. Readers must therefore always check the product information and clinical procedures with the most up to date published product information and data sheets provided by the manufacturers and the most recent codes of conduct and safety regulations. The authors and the publishers do not accept responsibility or legal liability for any errors in the text or for the misuse or misapplication of material in this work. Except where otherwise stated, drug dosages and recommendations are for the non-pregnant adult who is not breastfeeding.

Syndromes of the head and neck

Chapter:
Syndromes of the head and neck
Author(s):

Laura Mitchell,

David A. Mitchell

DOI:
10.1093/med/9780199553303.003.18

Contents

Introduction - Definitions - Albright syndrome - Apert syndrome - Beckwith–Wiedemann syndrome - Behçet syndrome - Binder syndrome - Chediak–Higashi syndrome - Cleidocranial dysostosis - ‘Cri du chat’ syndrome - Crouzon syndrome - Down syndrome - Eagle syndrome - Ehlers–Danlos syndrome - Frey syndrome - Gardener syndrome - Goldenhar syndrome - Gorlin–Goltz syndrome - Graves’ disease - Heerfordt syndrome - Hemifacial microsomia - ‘Histiocytosis-X’ - Horner syndrome - Hurler syndrome - Hypohydrotic ectodermal dysplasia - Kikuchi syndrome - Klippel–Feil anomalad - Larsen syndrome - Lesch–Nyhan syndrome - MAGIC syndrome - Marcus Gunn syndrome - Marfan syndrome - Melkerson–Rosenthal syndrome - Multiple endocrine neoplasia - Orofacial–digital syndrome - Papillon–Lefevre syndrome - Patterson–Brown–Kelly syndrome (Plummer–Vinson syndrome) - Peutz–Jeghers syndrome - Progeria - Pycnodysostosis - Ramsay Hunt syndrome - Reiter syndrome - Reyes syndrome - Robin sequence - Romberg syndrome - Sicca syndrome - Sjögren syndrome - Stevens–Johnson syndrome - Stickler syndrome - Sturge–Weber anomalad - Treacher–Collins syndrome - Trotter syndrome - Van der Woude syndrome - von Recklinghausen neurofibromatosis/syndrome

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