A color atlas of orofacial health and disease in children - download pdf or read online

By Crispian Scully, Richard Welbury, Catherine Flaitz, Oslei Paes de Almeida

ISBN-10: 0203215559

ISBN-13: 9780203215555

Like the winning first version, this superior, up to date and accelerated moment variation profiles the typical orofacial problems and quite a lot of much less universal and a few infrequent problems. the focal point is at the prevalence of those issues in teenagers and teenagers, and the writer tailors the remark to precise pediatric age teams. within the new version, the textual content contains therapy options for the commonest oral illnesses. Any surgeon known as upon to diagnose and deal with teenagers who've orofacial difficulties will enjoy the wealth of fabric provided here.

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Additional info for A color atlas of orofacial health and disease in children and adolescents: diagnosis and management

Sample text

122 Figure 122. Hypermobility of the joints in Ehlers–Danlos syndrome. Figure 124. Premature apical closure, cessation of root growth and intrapulpal calcification in Ehlers–Danlos syndrome. 121 Figure 121. Hyperelasticity of the skin in Ehlers–Danlos syndrome. 123 Figure 123. Because of the hyperelasticity of the skin, healing of skin lacerations over joints in Ehlers–Danlos syndrome can result in a very fine papyraceous scarring, as shown here. This easily breaks down and these lesions are best treated by a period of joint immobilization.

74 75 Figure 75. Same patient as in Figure 74 showing lymphangioma. Congenital and hereditable disorders with sole or prominent orofacial involvement 33 MELKERSSON–ROSENTHAL SYNDROME Melkersson–Rosenthal syndrome (Figs 76, 77) consists of facial paralysis, facial edema, fissured tongue and plicated mucosal swelling. Not all patients have every component of the syndrome, which is closely related to orofacial granulomatosis and oral Crohn’s disease. Management Reassurance only is usually required, but surgery may be indicated.

There is no staining for glycogen, lipid or amyloid. RETT SYNDROME Rett syndrome (Figs 88, 89) seen only in females is characterized by progressive neurological disorder, loss of purposeful hand use and acquired microcephaly. Constant bruxism is a conspicuous feature. Diagnosis Diagnosis is clinical. Management Reassurance only is usually required, but restorative dentistry and genetic counseling may be indicated. Diagnosis Diagnosis is clinical, supported by biopsy and biochemistry (assay of plasma plasminogen levels).

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A color atlas of orofacial health and disease in children and adolescents: diagnosis and management by Crispian Scully, Richard Welbury, Catherine Flaitz, Oslei Paes de Almeida


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